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

DIGILAB MODEL 1500 PERIMETER

K Number: K870120 · Decision Feb 20, 1987
Classifications
1
FEI Numbers
66
Registration Numbers
67
Same Product Code
40
Applicant Total
319
Review Days
39

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Basic Information

Device Name
DIGILAB MODEL 1500 PERIMETER
K Number
K870120
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
886.1605
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Applicant
Bio-Rad
Date Received
January 12, 1987
Decision Date
February 20, 1987
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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