Asclepion-Meditec AG - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
FDA 510(k) Regulatory Record - Asclepion-Meditec AG General & Plastic Surgery ✕
4 devices
Cleared
Sep 13, 2002
LASERSYSTEM BEAUTYSTAR 532
General & Plastic Surgery
88d
Cleared
Mar 08, 2002
DERMASTAR ER:YAG LASER SYSTEM
General & Plastic Surgery
88d
Cleared
Feb 26, 2002
LASER SYSTEM YELLOWSTAR
General & Plastic Surgery
89d
Cleared
Sep 11, 2000
C02 LASER MULTIPULSE
General & Plastic Surgery
70d