Candela Laser Corp. - FDA 510(k) Cleared Devices
43
Total
43
Cleared
0
Denied
Candela Laser Corp. has 43 FDA 510(k) cleared medical devices. Based in Wayland, US.
Historical record: 43 cleared submissions from 1988 to 1996. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Candela Laser Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Candela Laser Corp.
43 devices
Cleared
Aug 15, 1996
ANDELA DYNAMIC COOLING DEVICE
Physical Medicine
528d
Cleared
Jun 14, 1996
CANDELA Q-SWITCHED ALEXANDRITE LASERS
General & Plastic Surgery
185d
Cleared
Apr 03, 1996
CANDELA HCS 2000 URETHERAL WARMER CATHETER
General & Plastic Surgery
154d
Cleared
Feb 05, 1996
CANDELA CRYO-PROBE HOLDER
General & Plastic Surgery
104d
Cleared
Feb 02, 1996
CANDELA SPTL LONG PULSE/TUNABLE PULSED DYE LASE
General & Plastic Surgery
98d
Cleared
Oct 24, 1995
CANDELA MODEL PLTL-1 LASER SYSTEM
General & Plastic Surgery
96d
Cleared
Oct 18, 1995
CANDELA CRYOSYSTEM CS-5
General & Plastic Surgery
96d
Cleared
May 26, 1995
ALEXLAZR
General & Plastic Surgery
91d
Cleared
Mar 24, 1995
CANDELA RUBY LAZE Q-SWITCHED RUBY LASER
General & Plastic Surgery
93d
Cleared
Mar 10, 1995
CANDELA 10MM CIRCULAR SPOT LASER HANDPIECE
General & Plastic Surgery
25d
Cleared
Mar 09, 1995
CANDELA SPTL VARIABLE PULSE/TUNABLE PULSED DYE LASERS
General & Plastic Surgery
244d
Cleared
Mar 06, 1995
CANDELA URETHRAL/BLADDER SOUND
Gastroenterology & Urology
21d
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