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

OPTICOM M600

K Number: K932258 · Decision Jul 25, 1994
Classifications
1
FEI Numbers
66
Registration Numbers
67
Same Product Code
40
Applicant Total
10
Review Days
441

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Basic Information

Device Name
OPTICOM M600
K Number
K932258
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
886.1605
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Clement Clarke, Inc.
Date Received
May 10, 1993
Decision Date
July 25, 1994
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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