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FDA 510(k) Applications Submitted by JOAN CLIFFORD
FDA 510(k) Number
Submission Date
Device Name
Applicant
K010104
01/12/2001
CANDELA LONG PULSE ND:YAG
CANDELA CORP.
K011092
04/10/2001
CANDELA SPTL-1E PULSED DYE LASER
CANDELA CORP.
K002421
08/08/2000
CANDELA MID IR DIODE LASER SYSTEM
CANDELA CORP.
K013043
09/10/2001
CANDELA CLEARBEAM PULSED DYE LASER
CANDELA CORP.
K993671
11/01/1999
CANDELA SCLERO LONG PULSE DYE LASER
CANDELA CORP.
K001093
04/04/2000
CANDELA SPTL-1B PULSED DYE LASER
CANDELA CORP.
K001589
05/23/2000
CANDELA DYNAMIC COOLING DEVICE
CANDELA CORP.
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