Aesculap-Meditec North America - FDA 510(k) Cleared Devices
Recent clearances: LASER SYSTEM RUBYSTAR WITH Q-SWITCH AND NORMAL MODE, MEDITEC LINK, DERMABLATE ER: YAG LASER SYSTEM
6
Total
6
Cleared
0
Denied
FDA 510(k) Regulatory Record - Aesculap-Meditec North America General & Plastic Surgery ✕
4 devices
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