FDA 510(k) Applications Submitted by LORRAINE CALZETTA 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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