Medical Device Manufacturer · US , New York , NY

Moss Medical Products - FDA 510(k) Cleared Devices

8 submissions · 8 cleared · Since 1991

Recent clearances: Y2K2 ENTERNAL TUBE FLUID FILTER

8
Total
8
Cleared
0
Denied

Moss Medical Products has 8 FDA 510(k) cleared medical devices. Based in New York, US.

Historical record: 8 cleared submissions from 1991 to 2005. Primary specialty: Gastroenterology & Urology.

Browse the FDA 510(k) cleared devices submitted by Moss Medical Products Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.

FDA 510(k) Regulatory Record - Moss Medical Products

8 devices
1-8 of 8
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