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FDA 510(k)

VESTEX Apparel

K-Number: K180217 · 2018-05-18

ApplicantVestagen Protective Technologies, Inc.
Decision Date2018-05-18
Product CodeQBW
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

VESTEX Apparel is a medical device manufactured by Vestagen Protective Technologies, Inc.. It received FDA 510(k) clearance on 2018-05-18 under approval number K180217. The device is classified under product code QBW. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VESTEX Apparel?

VESTEX Apparel is a medical device that received FDA 510(k) clearance on 2018-05-18. It is manufactured by Vestagen Protective Technologies, Inc.. The 510(k) number is K180217.

When was VESTEX Apparel approved by the FDA?

VESTEX Apparel received FDA 510(k) clearance on 2018-05-18, under approval number K180217.

What company makes VESTEX Apparel?

VESTEX Apparel is manufactured by Vestagen Protective Technologies, Inc..

What is the FDA product code for VESTEX Apparel?

The FDA product code for VESTEX Apparel is QBW.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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