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FDA 510(k)

RejuvatoneMD

K-Number: K152199 · 2016-03-23

ApplicantTrophy Skin, Inc.
Decision Date2016-03-23
Product CodeNFO
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

RejuvatoneMD is a medical device manufactured by Trophy Skin, Inc.. It received FDA 510(k) clearance on 2016-03-23 under approval number K152199. The device is classified under product code NFO. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RejuvatoneMD?

RejuvatoneMD is a medical device that received FDA 510(k) clearance on 2016-03-23. It is manufactured by Trophy Skin, Inc.. The 510(k) number is K152199.

When was RejuvatoneMD approved by the FDA?

RejuvatoneMD received FDA 510(k) clearance on 2016-03-23, under approval number K152199.

What company makes RejuvatoneMD?

RejuvatoneMD is manufactured by Trophy Skin, Inc..

What is the FDA product code for RejuvatoneMD?

The FDA product code for RejuvatoneMD is NFO.

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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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