FDA 510(k) Applications Submitted by AESCULAP-MEDITEC GMBH

FDA 510(k) Number Submission Date Device Name Applicant
K991993 06/14/1999 PHACOLASE ER: YAG LASER AESCULAP-MEDITEC GMBH
K983215 09/14/1998 MULTIPULSE CO2 LASER AESCULAP-MEDITEC GMBH
K964128 10/15/1996 MCL 29 DERMABLATE ERBIUM LASER SYSTEM AESCULAP-MEDITEC GMBH


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