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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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