FDA 510(k)

Define RF Microneedling System

K-Number: K232301 · 2024-03-14

Decision Date2024-03-14

Product CodeGEI

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

Define RF Microneedling System is a medical device manufactured by Aesthetic Management Partners. It received FDA 510(k) clearance on 2024-03-14 under approval number K232301. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Define RF Microneedling System?

Define RF Microneedling System is a medical device that received FDA 510(k) clearance on 2024-03-14. It is manufactured by Aesthetic Management Partners. The 510(k) number is K232301.

When was Define RF Microneedling System approved by the FDA?

Define RF Microneedling System received FDA 510(k) clearance on 2024-03-14, under approval number K232301.

What company makes Define RF Microneedling System?

Define RF Microneedling System is manufactured by Aesthetic Management Partners.

What is the FDA product code for Define RF Microneedling System?

The FDA product code for Define RF Microneedling System is GEI.

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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.