KOWA VX-20— 510(k) K112330

Substantially Equivalent

Kowa Co. , Ltd.

FDA 510(k) clearance K112330 for KOWA VX-20, Substantially Equivalent on 2012-02-16. Applicant: Kowa Co. , Ltd.. Device class: 2.

Clearance details

Applicant: Kowa Co. , Ltd.
Product code: Code HKI
Device class: Class 2
Regulation: 21 CFR 886.1120
Advisory panel: Ophthalmic
Date received: 2011-08-12
Decision date: 2012-02-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Tokyo, JP

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.