FDA 510(k) Applications Submitted by WILLIAM T KELLEY

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
K002031 07/03/2000 PHACOFRAGMENTATION SYSTEM MEGATRON ASCLEPION-MEDITEC AG
K002032 07/03/2000 C02 LASER MULTIPULSE ASCLEPION-MEDITEC AG
K982548 07/21/1998 MLT 30 LASER MEDICAL LASER TECHNOLOGIES LTD.
K992536 07/29/1999 TECHNOSANAT KRYO TSK 2005 TECHNOSANAT INNOVATIVE MEDIZINTECHNIK GMBH
K992707 08/11/1999 MCL 29 DERMABLATE ER:YAG LASER SYSTEM AESCULAP-MEDITEC NORTH AMERICA
K013940 11/29/2001 LASER SYSTEM YELLOWSTAR ASCLEPION-MEDITEC AG
K994116 12/06/1999 LASER SYSTEM MEDIOSTAR H (WITH AND WITHOUT SKIN COOLING SYSTEM) AESCULAP-MEDITEC NORTH AMERICA
K014057 12/10/2001 DERMASTAR ER:YAG LASER SYSTEM ASCLEPION-MEDITEC AG
K980001 01/02/1998 JENASCAN JENOPTIK LASER, OPTIK, SYSTEME GMBH
K980361 01/29/1998 DERMABLATE ER: YAG LASER SYSTEM AESCULAP-MEDITEC NORTH AMERICA
K981196 03/19/1998 MEDITEC LINK AESCULAP-MEDITEC NORTH AMERICA
K991993 06/14/1999 PHACOLASE ER: YAG LASER AESCULAP-MEDITEC GMBH
K983215 09/14/1998 MULTIPULSE CO2 LASER AESCULAP-MEDITEC GMBH
K032910 09/22/2003 CARRIAZO PENDULAR SCHWIND EYE-TECH-SOLUTIONS GMBH & CO. KG
K964128 10/15/1996 MCL 29 DERMABLATE ERBIUM LASER SYSTEM AESCULAP-MEDITEC GMBH
K974467 11/26/1997 AESCULAP-MEDITEC SLIT LAMPS SL07 AND SL08 AESCULAP-MEDITEC NORTH AMERICA


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