KOWA VX-10I— 510(k) K062021

Substantially Equivalent

Kowa Co. , Ltd.

FDA 510(k) clearance K062021 for KOWA VX-10I, Substantially Equivalent on 2006-11-01. Applicant: Kowa Co. , Ltd..

Clearance details

Applicant: Kowa Co. , Ltd.
Product code: Code HKI
Advisory panel: Ophthalmic
Date received: 2006-07-17
Decision date: 2006-11-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Rockville, MD, US

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