FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

AUTOMATED PERIMETERS

K Number: K803159 · Decision Feb 4, 1981
Classifications
1
FEI Numbers
66
Registration Numbers
67
Same Product Code
40
Applicant Total
14
Review Days
58

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Basic Information

Device Name
AUTOMATED PERIMETERS
K Number
K803159
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
886.1605
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Applicant
Coburn Optical Ind., Inc.
Date Received
December 8, 1980
Decision Date
February 4, 1981
Product Code
HPT
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
HPT Perimeter, Automatic, Ac-Powered

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Other Clearances by Coburn Optical Ind., Inc.

K Number Device Name
K892351 MAGNILINK SYSTEM 602
K892350 MAGNILINK SYSTEM 402/5
K892349 MAGNILINK SYSTEM 209
K892347 MAGNILINK SYSTEM 101
K892348 MAGNILINK SYSTEM 201
K862188 IRRIGATION & ASPIRATION/VITRECTOMY DEVICE
K853457 COBURN I/A SYSTEM
K821737 DISP. MICROSURGICAL KNIVES
K812441 DI-CROWN
K801659 BIOPHTAL CLINICAL ENDOTHELIAL MICROSCOPE
Search all 14 clearances from Coburn Optical Ind., Inc. →