FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

CANDELA CBEAM PULSE DYE LASER SYSTEM

K Number: K033331 · Decision Jan 16, 2004
Classifications
1
FEI Numbers
476
Registration Numbers
479
Same Product Code
2793
Applicant Total
47
Review Days
92

Basic Information

Device Name
CANDELA CBEAM PULSE DYE LASER SYSTEM
K Number
K033331
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4810
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
CANDELA CORP.
Date Received
October 16, 2003
Decision Date
January 16, 2004
Product Code
GEX
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
GEX Powered Laser Surgical Instrument

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (GEX), ordered by most recent decision date.

View all

Other Clearances by CANDELA CORP.

K Number Device Name
K140732 CANDELA GENTLELASE FAMILY OF LASER SYSTEMS
K140122 CANDELA GENTLEMAX FAMILY OF LASER SYSTEM
K133283 CANDELA GENTLEMAX FAMILY OF LASER SYSTEMS
K112715 CANDELA GENTLEMAX FAMILY OF LASERS
K111144 CANDELA GENTLELASE FAMILY OF LASERS
K081324 CANDELA FAMILY OF Q-SWITCHED ALEXANDRITE LASERS
K073534 CANDELA FAMILY OF Q-SWITCHED ALEXANDRITE LASER (ALEXLAZR) SYSTEMS
K071469 INOLASE SERENITY PSF ( PNEUMATIC SKIN FLATTENING) SYSTEM
K063800 CANDELA FLUORESCENT PULSED LIGHT SYSTEM
K063074 CANDELA 3630 LASER SYSTEM
Search all 47 clearances from CANDELA CORP. →