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FDA 510(k) Applications Submitted by LORRAINE C PATROVIC
FDA 510(k) Number
Submission Date
Device Name
Applicant
K050673
03/15/2005
CANDELA FAMILY OF PULSE DYE LASER SYSTEMS
CANDELA CORP.
K030846
03/17/2003
CANDELA SMOOTHBEAM LASER SYSTEM
CANDELA CORP.
K041242
05/11/2004
CANDELA SMOOTHBEAM LASER SYSTEM
CANDELA CORP.
K051359
05/24/2005
CANDELA FAMILY OF PULSED DYE LASER SYSTEMS: PIGMENTED LESION HANDPIECE ACCESSORY
CANDELA CORP.
K033331
10/16/2003
CANDELA CBEAM PULSE DYE LASER SYSTEM
CANDELA CORP.
K033461
10/30/2003
CANDELA VBEAM PULSE DYE LASER SYSTEM
CANDELA CORP.
K033172
09/30/2003
CANDELA GENTLEYAG FAMILY OF LASER SYSTEMS
CANDELA CORP.
K030834
03/17/2003
CANDELA SMOOTHBEAM LASER SYSTEM
CANDELA CORP.
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