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.


Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact