Medical Device Manufacturer · CA , Richmond, Bc

Pm Devices, Inc. - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 2003

Recent clearances: PERIPATCH ENDO-SLEEVE, PERIPATCH SHEET, MODELS 1.5P8, 1.5P16, 4P4, 4P6, 6P8 AND 10P16, PERIPATCH SLEEVE, MODELS G35, E35, G45, E45, G60, E60, 5C6, 5C8, 5C10

4
Total
4
Cleared
0
Denied

Pm Devices, Inc. has 4 FDA 510(k) cleared medical devices. Based in Richmond, Bc, CA.

Historical record: 4 cleared submissions from 2003 to 2007. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by Pm Devices, Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Pm Devices, Inc.

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