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FDA 510(k)

KOWA VX-10 A

K-Number: K091683 · 2009-07-02

Decision Date2009-07-02
Product CodeHKI
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

KOWA VX-10 A is the device name listed in this FDA 510(k) record. The listed applicant is Kowa Co. , Ltd.. It received FDA 510(k) clearance on 2009-07-02 under 510(k) number K091683. The device is classified under product code HKI. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 15 devices →

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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