FDA 510(k) Substantially Equivalent 🇺🇸 United States

COOPER LASERSONICS ND:YAG LASER 8000

K Number: K841793 · Decision Jun 7, 1984
Classifications
0
FEI Numbers
0
Registration Numbers
0
Same Product Code
0
Applicant Total
54
Review Days
38

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Basic Information

Device Name
COOPER LASERSONICS ND:YAG LASER 8000
K Number
K841793
Clearance Type
Traditional
Decision
Substantially Equivalent
Applicant
Cooper Lasersonics, Inc.
Date Received
April 30, 1984
Decision Date
June 7, 1984
Advisory Committee
Unknown
Review Advisory Committee
CV
Third Party
N

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. →