Siemens wins FDA clearance for Multix Impact DR unit
January 22, 2019 -- Siemens Healthineers has garnered U.S. Food and Drug Administration (FDA) clearance for its Multix Impact floor-mounted digital radiography (DR) system.
January 22, 2019 -- Siemens Healthineers has garnered U.S. Food and Drug Administration (FDA) clearance for its Multix Impact floor-mounted digital radiography (DR) system.
RadioMedix lands $2M grant from NCI
January 22, 2019 -- Biotechnology firm RadioMedix has received a two-year $2 million grant from the U.S. National Cancer Institute (NCI) to support the clinical development of targeted alpha-emitter therapy for neuroendocrine tumors.
January 22, 2019 -- Biotechnology firm RadioMedix has received a two-year $2 million grant from the U.S. National Cancer Institute (NCI) to support the clinical development of targeted alpha-emitter therapy for neuroendocrine tumors.
Carestream readies new clinical collaboration software
January 22, 2019 -- Carestream Health will present the latest release of its Vue Clinical Collaboration Platform software at next month's annual Healthcare Information and Management Systems Society meeting in Orlando, FL.
January 22, 2019 -- Carestream Health will present the latest release of its Vue Clinical Collaboration Platform software at next month's annual Healthcare Information and Management Systems Society meeting in Orlando, FL.
iSchemaView, Samsung NeuroLogica join forces
January 22, 2019 -- Cerebrovascular imaging software developer iSchemaView has formed a partnership with Samsung NeuroLogica.
January 22, 2019 -- Cerebrovascular imaging software developer iSchemaView has formed a partnership with Samsung NeuroLogica.
IRadimed temporarily halts European sales of monitor
January 22, 2019 -- MRI accessories developer IRadimed has temporarily suspended shipments of its 3880 MRI-compatible patient vital signs monitoring systems in European markets following the expiration of its CE Mark on January 17.
January 22, 2019 -- MRI accessories developer IRadimed has temporarily suspended shipments of its 3880 MRI-compatible patient vital signs monitoring systems in European markets following the expiration of its CE Mark on January 17.
ASE releases clinical guidelines for TTE
January 22, 2019 -- The American Society of Echocardiography (ASE) has released new guidelines for performing comprehensive transthoracic echocardiographic (TTE) exams.
January 22, 2019 -- The American Society of Echocardiography (ASE) has released new guidelines for performing comprehensive transthoracic echocardiographic (TTE) exams.
Formlabs introduces elastic resin for 3D-printed models
January 21, 2019 -- 3D printer manufacturer Formlabs has created a soft and pliable -- yet durable -- material that clinicians can use to make anatomical models with desktop 3D printers.
January 21, 2019 -- 3D printer manufacturer Formlabs has created a soft and pliable -- yet durable -- material that clinicians can use to make anatomical models with desktop 3D printers.
FDA issues warning on PAD vascular balloon, stent
January 18, 2019 -- The U.S. Food and Drug Administration (FDA) has issued a warning to healthcare professionals about the use of certain drug-containing balloons and stents in patients with peripheral arterial disease (PAD).
January 18, 2019 -- The U.S. Food and Drug Administration (FDA) has issued a warning to healthcare professionals about the use of certain drug-containing balloons and stents in patients with peripheral arterial disease (PAD).
Medtronic recalls StealthStation brain imaging software
January 18, 2019 -- Device manufacturer Medtronic is recalling its Synergy and StealthStation S7 cranial software applications for its StealthStation surgical navigation system, according to a statement from the U.S. Food and Drug Administration.
January 18, 2019 -- Device manufacturer Medtronic is recalling its Synergy and StealthStation S7 cranial software applications for its StealthStation surgical navigation system, according to a statement from the U.S. Food and Drug Administration.
FDA clears Hologic's Localizer for long-term placement
January 18, 2019 -- The U.S. Food and Drug Administration (FDA) has cleared women's imaging firm Hologic's Localizer radiofrequency identification breast lesion localization device for long-term placement.
January 18, 2019 -- The U.S. Food and Drug Administration (FDA) has cleared women's imaging firm Hologic's Localizer radiofrequency identification breast lesion localization device for long-term placement.