Pm Devices, Inc. is one of 208 FDA 510(k) medical device manufacturers from Canada in the dataset, ranked by real submission volume.
Pm Devices, Inc. - FDA 510(k) Cleared Devices
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.
4 devices
Cleared
Mar 20, 2007
PERIPATCH ENDO-SLEEVE
General & Plastic Surgery
113d
Cleared
Jun 15, 2004
PERIPATCH SHEET, MODELS 1.5P8, 1.5P16, 4P4, 4P6, 6P8 AND 10P16
General & Plastic Surgery
76d
Cleared
Jun 04, 2004
PERIPATCH SLEEVE, MODELS G35, E35, G45, E45, G60, E60, 5C6, 5C8, 5C10
General & Plastic Surgery
164d
Cleared
Sep 16, 2003
PERIPATCH SHEET, MODELS 1.5P8, 4P4, 4P6, 6P8, 10P16, 1.5P16
Cardiovascular
84d