Medical Device Manufacturer · US , Potomac , MD

Perstorp AB C/O Robert Joel Slomoff - FDA 510(k) Cleared Devices

2 submissions · 1 cleared · Since 1987

2

Total

1

Cleared

0

Denied

FDA 510(k) Regulatory Record - Perstorp AB C/O Robert Joel Slomoff General & Plastic Surgery ✕

2 devices

1-2 of 2

Cleared Jan 31, 1991

General & Plastic Surgery · 83d

Cleared Mar 20, 1987

IODOSORB POWDER

General & Plastic Surgery · 38d