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FDA 510(k) Applications Submitted by AESCULAP-MEDITEC NORTH AMERICA
FDA 510(k) Number
Submission Date
Device Name
Applicant
K991285
04/15/1999
LASER SYSTEM RUBYSTAR WITH Q-SWITCH AND NORMAL MODE
AESCULAP-MEDITEC NORTH AMERICA
K992707
08/11/1999
MCL 29 DERMABLATE ER:YAG LASER SYSTEM
AESCULAP-MEDITEC NORTH AMERICA
K994116
12/06/1999
LASER SYSTEM MEDIOSTAR H (WITH AND WITHOUT SKIN COOLING SYSTEM)
AESCULAP-MEDITEC NORTH AMERICA
K980361
01/29/1998
DERMABLATE ER: YAG LASER SYSTEM
AESCULAP-MEDITEC NORTH AMERICA
K981196
03/19/1998
MEDITEC LINK
AESCULAP-MEDITEC NORTH AMERICA
K974467
11/26/1997
AESCULAP-MEDITEC SLIT LAMPS SL07 AND SL08
AESCULAP-MEDITEC NORTH AMERICA
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