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

COOPER LASERSONICS 880 CO2/ND:YAG MEDICAL LASER SY

K Number: K851000 · Decision Aug 14, 1985
Classifications
1
FEI Numbers
476
Registration Numbers
479
Same Product Code
2793
Applicant Total
54
Review Days
156

Basic Information

Device Name
COOPER LASERSONICS 880 CO2/ND:YAG MEDICAL LASER SY
K Number
K851000
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4810
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
COOPER LASERSONICS, INC.
Date Received
March 11, 1985
Decision Date
August 14, 1985
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 COOPER LASERSONICS, INC.

K Number Device Name
K880807 ILLUMINA MODEL 25 CO2 LASER FOR GENERAL/PLASTIC SU
K880429 ILLUMINA 55 CO2 LASER SYSTEM
K880808 ILLUMINA MODEL 40 CO2 LASER FOR GENERAL/PLASTIC SU
K880809 ILLUMINA MODEL 55 CO2 LASER FOR GENERAL/PLASTIC SU
K880427 ILLUMINA 40 CO2 LASER SYSTEM
K880428 ILLUMINA 25 CO2 LASER SYSTEM
K880171 MODEL 4900 ND:YAG LASER FOR GASTRO & GENITOUR APPL
K880173 MODEL 4900 ND:YAG LASER FOR ENDOMETRIAL ABLATION
K880170 MODEL 4900 ND:YAG LASER FOR PULMONARY OBSTRUCTIONS
K880172 MODEL 4900 ND:YAG LASER FOR NEUROSURGERY APPLICA.
Search all 54 clearances from COOPER LASERSONICS, INC. →