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FDA 510(k)

Avazzia

K-Number: K162392 · 2017-05-12

ApplicantAvazzia, Inc.
Decision Date2017-05-12
Product CodeNUH
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

Avazzia is a medical device manufactured by Avazzia, Inc.. It received FDA 510(k) clearance on 2017-05-12 under approval number K162392. The device is classified under product code NUH. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Avazzia?

Avazzia is a medical device that received FDA 510(k) clearance on 2017-05-12. It is manufactured by Avazzia, Inc.. The 510(k) number is K162392.

When was Avazzia approved by the FDA?

Avazzia received FDA 510(k) clearance on 2017-05-12, under approval number K162392.

What company makes Avazzia?

Avazzia is manufactured by Avazzia, Inc..

What is the FDA product code for Avazzia?

The FDA product code for Avazzia is NUH.

Other Devices by Avazzia, Inc.

K191951Avazzia OTC TENS for aesthetics, model BEST-AV1™: EZZI-LIFT™ Device

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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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