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

AUTOKERATOMETER, INSTRUMENT

K Number: K781994 · Decision Feb 12, 1979
Classifications
1
FEI Numbers
17
Registration Numbers
18
Same Product Code
28
Applicant Total
9
Review Days
75

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Basic Information

Device Name
AUTOKERATOMETER, INSTRUMENT
K Number
K781994
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
886.1350
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Applicant
Zeiss Humphrey System
Date Received
November 29, 1978
Decision Date
February 12, 1979
Product Code
HLQ
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
HLQ Keratoscope, Ac-Powered

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Other Clearances by Zeiss Humphrey System

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
K782096 INSTRUMENTS, OVERREFRACTION SYSTEM