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

ANOMALOSCOPE QUADRANT TEST-6

K Number: K913962 · Decision Oct 23, 1991
Classifications
1
FEI Numbers
5
Registration Numbers
5
Same Product Code
2
Applicant Total
8
Review Days
48

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Basic Information

Device Name
ANOMALOSCOPE QUADRANT TEST-6
K Number
K913962
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
886.1070
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Lkc Technologies, Inc.
Date Received
September 5, 1991
Decision Date
October 23, 1991
Product Code
HIW
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
HIW Anomaloscope

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Other Clearances by Lkc Technologies, Inc.

K Number Device Name
K142567 RETeval Visual Electrodiagnostic Device
K914163 SCOPTOPIC SENSITIVITY TEST-1[SST-1]
K875026 ANOMALOSCOPE PLATE TEST - 5 [APT-5]
K874336 PATTERN DISCRIMINATION PERIMETER
K820414 UNIVERSAL TESTING & ANALYSIS SYSTEMS
K790109 TELEMETRY, BIOMEDICAL
K760199 ELECTRORETINOGRAPH