FDA 510(k) FDA class 2 Substantially Equivalent 🇬🇧 United Kingdom

PERKINS HAND-HELD APPLANATION TONOMETER

K Number: K961512 · Decision Jul 18, 1996
Classifications
1
FEI Numbers
64
Registration Numbers
64
Same Product Code
55
Applicant Total
10
Review Days
90

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Basic Information

Device Name
PERKINS HAND-HELD APPLANATION TONOMETER
K Number
K961512
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
886.1930
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Clement Clarke, Inc.
Date Received
April 19, 1996
Decision Date
July 18, 1996
Product Code
HKY
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
HKY Tonometer, Manual

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