RejuvatoneMD
K-Number: K152199 · 2016-03-23
Device Summary
Frequently Asked Questions
What is the RejuvatoneMD?
RejuvatoneMD is a medical device that received FDA 510(k) clearance on 2016-03-23. The listed applicant is Trophy Skin, Inc.. The 510(k) number is K152199.
When did RejuvatoneMD receive FDA 510(k) clearance?
RejuvatoneMD received FDA 510(k) clearance on 2016-03-23, under 510(k) number K152199.
Who is the listed applicant for RejuvatoneMD?
The FDA 510(k) record lists Trophy Skin, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for RejuvatoneMD?
The FDA product code for RejuvatoneMD is NFO.
Related Devices (Code: NFO)
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.