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FDA 510(k)

Define RF Microneedling System

K-Number: K232301 · 2024-03-14

ApplicantAesthetic Management Partners
Decision Date2024-03-14
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Define RF Microneedling System is the device name listed in this FDA 510(k) record. The listed applicant is Aesthetic Management Partners. It received FDA 510(k) clearance on 2024-03-14 under 510(k) 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. The listed applicant is Aesthetic Management Partners. The 510(k) number is K232301.

When did Define RF Microneedling System receive FDA 510(k) clearance?

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

Who is the listed applicant for Define RF Microneedling System?

The FDA 510(k) record lists Aesthetic Management Partners as the applicant. This does not by itself establish the device manufacturer.

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

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

Related Devices (Code: GEI)

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.

K261179AlphaTriPart - Monopolar MIC InstrumentsGimmi GmbHK253504Volnewmer™Classys, Inc.K254056THUNDERBEAT 5 mm, 45 cm, Front-actuated Grip Type S (TB-0545FCS); THUNDERBEAT 5 mm, 35 cm, Front-actuated Grip Type S (TB-0535FCS); THUNDERBEAT 5 mm, 20 cm, Front-actuated Grip Type S (TB-0520FCS)Olympus Medical Systems Corp.K253484LUTRONIC GENIUSCynosure Lutronic Technology CorporationK251492Irrigation Tubing Bipolar Cord SetNew Deantronics Taiwan , Ltd.K260636Remanufactured LigaSure XP Maryland Jaw Sealer/Divider Without Nano-coatingStryker Sustainability Solutions

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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