Philips Volcano obtains CE mark approval for iFR Scout pullback software
Netherlands-based Royal Philips business Volcano has obtained CE mark approval for its iFR Scout pullback software. The new software, which […]
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Medtronic launches PoleStar MRI System in USA
Medtronic has launched its PoleStar N30 Surgical MRI system in the USA as a device to help optimise tumour procedures during neurosurgery after getting US Food & Drug Administration (FDA) 510(K) clearance.
FDA Issues Guidance to Infusion Pump Manufacturers
The US Food & Drug Administration (FDA) has issued new guidance and letters to infusion pump manufacturers as part of an initiative to institute stricter pre-market requirements.
FDA Launches Home-Use Medical Devices Safety Initiative
The US Food & Drug Administration (FDA) has launched a new initiative to improve the safety of complex home-use medical devices such as hemodialysis systems, wound care and intravenous therapy devices.
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Flipkart Health+ App Launched
06-04-2022
