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

ARGON/KRYPTON LASER SYSTEM 8500

K Number: K844209 · Decision Feb 6, 1985
Classifications
1
FEI Numbers
26
Registration Numbers
27
Same Product Code
29
Applicant Total
54
Review Days
98

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Basic Information

Device Name
ARGON/KRYPTON LASER SYSTEM 8500
K Number
K844209
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
886.4690
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Applicant
Cooper Lasersonics, Inc.
Date Received
October 31, 1984
Decision Date
February 6, 1985
Product Code
HQB
Advisory Committee
Ophthalmic
Review Advisory Committee
OP
Third Party
N

Classifications

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

Product Code Device Name
HQB Photocoagulator And Accessories

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Other Clearances by Cooper Lasersonics, Inc.

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