510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K954781Substantially Equivalent

Kowa Genesis Hand-Held Fundus Camera

Kowa Pharmaceuticals America, Inc., Washington DC / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K954781 is the FDA 510(k) clearance record for KOWA GENESIS HAND-HELD FUNDUS CAMERA, a class II device, cleared for Kowa Optimed, Inc. on under FDA product code HKI (Camera, Ophthalmic, Ac-Powered). FDA records list 10 510(k) clearances for Kowa Pharmaceuticals America, Inc., from to . As of , FDA records show no recalls naming K954781.

Clearance record

Decision date
Received
(45 days to decision)
Product code
HKI Camera, Ophthalmic, Ac-Powered
Regulation
21 CFR 886.1120
Device class
Class II
Review panel
Ophthalmic
Applicant
Kowa Optimed, Inc. 700 Thirteenth St. N.W, Washington DC
510(k) summary
Statement
Third party review
No

Clearances, product code HKI

Trailing 12 months
3 clearances under product code HKI in the twelve months to October 2026, December 2025 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code HKI, trailing twelve months
MonthClearances
November 20250
December 20251
January 20261
February 20260
March 20260
April 20260
May 20260
June 20261
July 20260
August 20260
September 20260
October 20260