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510(k) K062356

KOWA NONMYD ALPHA-D by Kowa Co. , Ltd. — Product Code HKI

K062356 is an FDA 510(k) premarket notification submitted by Kowa Co. , Ltd. for the device "KOWA NONMYD ALPHA-D". The FDA issued a decision of Substantially Equivalent on September 27, 2006. The device falls under product code HKI (Camera, Ophthalmic, Ac-Powered), a Class II device regulated under 21 CFR 886.1120. Kowa Co. , Ltd. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
September 27, 2006
Date Received
August 14, 2006
Clearance Type
Special
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Camera, Ophthalmic, Ac-Powered
Device Class
Class II
Regulation Number
886.1120
Review Panel
OP
Submission Type

Other clearances by Kowa Co. , Ltd.

  • K133755 — KOWA SL-17 (March 11, 2014)
  • K112330 — KOWA VX-20 (February 16, 2012)
  • K101628 — KOWA NONMYD WX (January 26, 2011)
  • K091098 — KOWAGENESIS-DF (August 7, 2009)
  • K091039 — KOWA, FM-600, MODEL LSS50 (August 7, 2009)
  • K091683 — KOWA VX-10 A (July 2, 2009)
  • K083387 — MODIFICATION TO KOWA NONMYD ALPHA-DIII (January 16, 2009)
  • K082767 — KOWA NONMYD ALPHA-DIII (October 21, 2008)
  • K080681 — KOWA GENESIS-D (April 4, 2008)
  • K063640 — KOWA SL-15 (December 18, 2006)

Other clearances for product code HKI

  • K253176 — TearView (June 22, 2026)
  • K251353 — Eyer 2 (January 16, 2026)
  • K252120 — Fundus On Phone Non Mydriatic (FOP NM-10) (December 12, 2025)
  • K250770 — Optina-4C (MHRC-C1N) (September 4, 2025)
  • K243600 — 3nethra neo HD FA; 3nethra neo HD (August 14, 2025)
  • K250683 — Resolve Fundus Camera (April 30, 2025)
  • K243664 — Sentinel Camera (December 17, 2024)
  • K242508 — Verily Numetric Retinal Camera (December 9, 2024)
  • K241049 — CANON Fundus Camera CR-10 (CR-10) (May 15, 2024)
  • K231230 — Optina-4C (MHRC-C1N) (December 5, 2023)

FDA data resources