FDA 510(k) FDA class 2 Substantially Equivalent 🇯🇵 Japan

KOWA VX-10 A

K Number: K091683 · Decision Jul 2, 2009
Classifications
1
FEI Numbers
65
Registration Numbers
66
Same Product Code
155
Applicant Total
16
Review Days
22

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Basic Information

Device Name
KOWA VX-10 A
K Number
K091683
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
886.1120
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Kowa Co. , Ltd.
Date Received
June 10, 2009
Decision Date
July 2, 2009
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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Other Clearances by Kowa Co. , Ltd.

K Number Device Name
K133755 KOWA SL-17
K112330 KOWA VX-20
K101628 KOWA NONMYD WX
K091098 KOWAGENESIS-DF
K091039 KOWA, FM-600, MODEL LSS50
K083387 MODIFICATION TO KOWA NONMYD ALPHA-DIII
K082767 KOWA NONMYD ALPHA-DIII
K080681 KOWA GENESIS-D
K063640 KOWA SL-15
K062021 KOWA VX-10I
Search all 16 clearances from Kowa Co. , Ltd. →