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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