Medical Device Manufacturer · US , Coto De Caza , CA

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

6 submissions · 6 cleared · Since 1998

Recent clearances: LASER SYSTEM MEDIOSTAR H (WITH AND WITHOUT SKIN COOLING SYSTEM), MCL 29 DERMABLATE ER:YAG LASER SYSTEM, LASER SYSTEM RUBYSTAR WITH Q-SWITCH AND NORMAL MODE

View 6 510(k) Devices ↓

6

Total

6

Cleared

0

Denied

FDA 510(k) Regulatory Record - Aesculap-Meditec North America Ophthalmic ✕

2 devices

1-2 of 2

Cleared Jun 17, 1998

Ophthalmic · 90d

Cleared Feb 19, 1998

AESCULAP-MEDITEC SLIT LAMPS SL07 AND SL08

Ophthalmic · 85d