NEW YORK – Paige said on Tuesday that it has secured US Food and Drug Administration 510(k) clearance for the use of the company's FullFocus digital pathology image viewer with scanners from Leica and ...

Accelerate your tech game Paid Content How the New Space Race Will Drive Innovation How the metaverse will change the future of work and society Managing the Multicloud The Future of the Internet ...

Looking for the best piano keyboard for beginners? Well MusicRadar has you covered with expert advice and useful recommendations from industry professionals It has never been easier - or cheaper - to ...

If you continue to have this issue please contact customerservice@slackinc.com. Smith & Nephew received FDA 510(k) clearance of a stemless option for its Aetos shoulder system. The solution is ...

Incase, the brand that took over Microsoft’s accessories line, has revealed a compact ergonomic keyboard designed by the company. With a price of $119.99, the wireless keyboard features a split ...

Incase, the design brand now selling PC accessories designed by Microsoft has just announced a new Compact Ergonomic Keyboard. This new keyboard looks quite similar to the now-discontinued Surface ...

Inogen, Inc. INGN recently announced the FDA 510(k) clearance for the SIMEOX 200 Airway Clearance Device. The clearance is likely to expand INGN’s ability to market the device and meet the ...

FDA 510k Clearance provides a competitive edge. Manufacturers that achieve clearance for their medical devices can differentiate themselves in both local and international markets, especially in ...

(Nasdaq: MBOT), developer of the innovative LIBERTY® Endovascular Robotic System, concludes 2024 with the achievement of several key milestones, including the recent FDA 510(k) submission for FDA ...

(RTTNews) - Inogen, Inc. (INGN), Monday announced that the company has received U.S. Food and Drug Administration 510(k) clearance for the SIMEOX 200 Airway Clearance Device, designed to help ...

today announced that it has received U.S. Food and Drug Administration (FDA) 510(k) clearance for the SIMEOX 200 Airway Clearance Device, expanding the company’s ability to market and meet the ...