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

HUMPHREY IMAGE ANALYZER MODEL 110

K Number: K852638 · Decision Aug 12, 1985
Classifications
1
FEI Numbers
65
Registration Numbers
66
Same Product Code
155
Applicant Total
9
Review Days
53

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Basic Information

Device Name
HUMPHREY IMAGE ANALYZER MODEL 110
K Number
K852638
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
886.1120
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Applicant
Zeiss Humphrey System
Date Received
June 20, 1985
Decision Date
August 12, 1985
Product Code
HKI
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
HKI Camera, Ophthalmic, Ac-Powered

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K852639 HUMPHREY FIELD ANALYZER MODEL 630
K821940 THE HUMPHREY FIELD ANALYZER MODEL 610
K802029 OBJECTIVE REFRACTOR
K781994 AUTOKERATOMETER, INSTRUMENT
K782096 INSTRUMENTS, OVERREFRACTION SYSTEM