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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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