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

INSTRUMENTS, OVERREFRACTION SYSTEM

K Number: K782096 · Decision Jan 26, 1979
Classifications
1
FEI Numbers
64
Registration Numbers
65
Same Product Code
15
Applicant Total
9
Review Days
39

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Basic Information

Device Name
INSTRUMENTS, OVERREFRACTION SYSTEM
K Number
K782096
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
886.1425
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Applicant
Zeiss Humphrey System
Date Received
December 18, 1978
Decision Date
January 26, 1979
Product Code
HLM
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
HLM Instrument, Measuring, Lens, Ac-Powered

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K Number Device Name
K942439 ZEISS OPMILAS 144 SURGICAL LASERS
K923211 DIGITAL OPHTHALMIC ULTRASOUND BIOMICROSCOPE
K923348 OPHTHALMIC A/B SCAN SYSTEM, MODEL 835 -- MODIFIED
K852639 HUMPHREY FIELD ANALYZER MODEL 630
K852638 HUMPHREY IMAGE ANALYZER MODEL 110
K821940 THE HUMPHREY FIELD ANALYZER MODEL 610
K802029 OBJECTIVE REFRACTOR
K781994 AUTOKERATOMETER, INSTRUMENT