FDA 510(k) Applications Submitted by LORRAINE NELSON

FDA 510(k) Number Submission Date Device Name Applicant
K020958 03/25/2002 CANDELA CBEAM PULSED DYE LASER SYSTEM CANDELA CORP.
K021180 04/15/2002 CANDELA VBEAM PULSED DYE LASER SYSTEM CANDELA CORP.
K022923 09/04/2002 CANDELA GENTLE YAG LASER SYSTEM CANDELA CORP.
K022951 09/05/2002 CANDELA GENTLE YAG LASER SYSTEM, VARIABLE PULSE YAG CANDELA CORP.
K013825 11/19/2001 CANDELA SMOOTHBEAM LASER SYSTEM CANDELA CORP.
K014128 12/17/2001 CANDELA SMOOTHBEAM LASER SYSTEM CANDELA CORP.


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