Medical Device Manufacturer · US , Great Neck , NY

Preswede AB - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2003

Recent clearances: POWERLITE 600 EX SYSTEM, POWERLITE 600 EP SYSTEM

View 2 510(k) Devices ↓

2

Total

2

Cleared

0

Denied

FDA 510(k) Regulatory Record - Preswede AB General & Plastic Surgery ✕

2 devices

1-2 of 2

Cleared Mar 16, 2004

POWERLITE 600 EX SYSTEM

General & Plastic Surgery · 88d

Cleared May 09, 2003

POWERLITE 600 EP SYSTEM

General & Plastic Surgery · 88d