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

KOWA HAND-HELD APPLANATION TONOMETER HA-1

K Number: K960924 · Decision Jun 4, 1996
Classifications
1
FEI Numbers
64
Registration Numbers
64
Same Product Code
55
Applicant Total
10
Review Days
90

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Basic Information

Device Name
KOWA HAND-HELD APPLANATION TONOMETER HA-1
K Number
K960924
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
886.1930
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Kowa Optimed, Inc.
Date Received
March 6, 1996
Decision Date
June 4, 1996
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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Other Clearances by Kowa Optimed, Inc.

K Number Device Name
K013805 KOWA AUTOMATED TONOMETER KT-500
K961090 AUTOMATIC VISUAL FIELD PLOTTER AP-125
K955442 KOWA SC-1200 PHOTO SLIT LAMP SYSTEM
K954781 KOWA GENESIS HAND-HELD FUNDUS CAMERA
K954780 KOWA PROFESSIONAL FUNDUS CAMERA MODELS FX-500, FX-500S, FX-500C
K954782 KOWA PORTABLE SLIT LAMP SL-14 & SL-14B
K913852 LASER FLARE METER
K880920 LASER FLARE CELL METER FC-1000
K881219 AUTOMATIC PERIMETER, AP-340