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

KOWA, FM-600, MODEL LSS50

K Number: K091039 · Decision Aug 7, 2009
Classifications
1
FEI Numbers
13
Registration Numbers
14
Same Product Code
21
Applicant Total
16
Review Days
116

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Basic Information

Device Name
KOWA, FM-600, MODEL LSS50
K Number
K091039
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
886.1570
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Kowa Co. , Ltd.
Date Received
April 13, 2009
Decision Date
August 7, 2009
Product Code
MYC
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
MYC Ophthalmoscope, Laser, Scanning

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (MYC), ordered by most recent decision date.

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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
K091683 KOWA VX-10 A
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. →