Pm Devices, Inc. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
FDA 510(k) Regulatory Record - Pm Devices, Inc. General & Plastic Surgery ✕
3 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