FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

OCU-FILM TIP COVER

K Number: K882750 · Decision Aug 4, 1988
Classifications
1
FEI Numbers
64
Registration Numbers
64
Same Product Code
55
Applicant Total
7
Review Days
30

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Basic Information

Device Name
OCU-FILM TIP COVER
K Number
K882750
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
886.1930
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Applicant
Oculab, Inc.
Date Received
July 5, 1988
Decision Date
August 4, 1988
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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K860061 OCULAB BIOMETRICPEN
K860062 OCULAB PACHPEN
K852774 OCULAB TONOPEN