Medical Device Manufacturer · US , Coto De Caza , CA

Aesculap-Meditec North America - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 1998

6

Total

6

Cleared

0

Denied

FDA 510(k) Regulatory Record - Aesculap-Meditec North America General & Plastic Surgery ✕

4 devices

1-4 of 4

Cleared Jun 01, 2000

LASER SYSTEM MEDIOSTAR H (WITH AND WITHOUT SKIN COOLING SYSTEM)

General & Plastic Surgery · 178d

Cleared Oct 19, 1999

MCL 29 DERMABLATE ER:YAG LASER SYSTEM

General & Plastic Surgery · 69d

Cleared Jul 12, 1999

LASER SYSTEM RUBYSTAR WITH Q-SWITCH AND NORMAL MODE

General & Plastic Surgery · 88d

Cleared Apr 21, 1998

DERMABLATE ER: YAG LASER SYSTEM

General & Plastic Surgery · 82d