Aesculap-Meditec North America

Aesculap-Meditec North America holds 6 FDA 510(k) medical device clearances, first cleared 1998, most recent 2000.

Top product codes for Aesculap-Meditec North America

Recent clearances by Aesculap-Meditec North America

K994116 — LASER SYSTEM MEDIOSTAR H (WITH AND WITHOUT SKIN COOLING SYSTEM)Code GEX·2000-06-01
K992707 — MCL 29 DERMABLATE ER:YAG LASER SYSTEMCode GEX·1999-10-19
K991285 — LASER SYSTEM RUBYSTAR WITH Q-SWITCH AND NORMAL MODECode GEX·1999-07-12
K981196 — MEDITEC LINKCode HQF·1998-06-17
K980361 — DERMABLATE ER: YAG LASER SYSTEMCode GEX·1998-04-21
K974467 — AESCULAP-MEDITEC SLIT LAMPS SL07 AND SL08Code HJO·1998-02-19

Data sourced from openFDA. This site is unofficial and independent of the FDA.