KOWA VX-10 A
K-Number: K091683 · 2009-07-02
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Device Summary
Frequently Asked Questions
What is the KOWA VX-10 A?
KOWA VX-10 A is a medical device that received FDA 510(k) clearance on 2009-07-02. The listed applicant is Kowa Co. , Ltd.. The 510(k) number is K091683.
When did KOWA VX-10 A receive FDA 510(k) clearance?
KOWA VX-10 A received FDA 510(k) clearance on 2009-07-02, under 510(k) number K091683.
Who is the listed applicant for KOWA VX-10 A?
The FDA 510(k) record lists Kowa Co. , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for KOWA VX-10 A?
The FDA product code for KOWA VX-10 A is HKI.
Other records listing Kowa Co. , Ltd. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: HKI)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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