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FDA 510(k)

Stivax

K-Number: K152571 · 2016-05-26

ApplicantBiegler GmbH
Decision Date2016-05-26
Product CodeBWK
DecisionSubstantially Equivalent

Device Summary

Stivax is a medical device manufactured by Biegler GmbH. It received FDA 510(k) clearance on 2016-05-26 under approval number K152571. The device is classified under product code BWK. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Stivax?

Stivax is a medical device that received FDA 510(k) clearance on 2016-05-26. It is manufactured by Biegler GmbH. The 510(k) number is K152571.

When was Stivax approved by the FDA?

Stivax received FDA 510(k) clearance on 2016-05-26, under approval number K152571.

What company makes Stivax?

Stivax is manufactured by Biegler GmbH.

What is the FDA product code for Stivax?

The FDA product code for Stivax is BWK.

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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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