FDA 510(k)

F Care RF System (00MEDRF4000US, 05RAFAELOPROBE, 05SPHERAPROBE, 06OUTPUTKAB, 06Pedal1St)

Numéro K : K252704 · 2025-11-24

Date de décision2025-11-24

Code produitGEI

Comité consultatifSU

DécisionSubstantially Equivalent

Résumé du dispositif

F Care RF System (00MEDRF4000US, 05RAFAELOPROBE, 05SPHERAPROBE, 06OUTPUTKAB, 06Pedal1St) is the device name listed in this FDA 510(k) record. The listed applicant is F Care Systems USA, LLC. It received FDA 510(k) clearance on 2025-11-24 under 510(k) number K252704. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Questions fréquentes

What is the F Care RF System (00MEDRF4000US, 05RAFAELOPROBE, 05SPHERAPROBE, 06OUTPUTKAB, 06Pedal1St)?

F Care RF System (00MEDRF4000US, 05RAFAELOPROBE, 05SPHERAPROBE, 06OUTPUTKAB, 06Pedal1St) is a medical device that received FDA 510(k) clearance on 2025-11-24. The listed applicant is F Care Systems USA, LLC. The 510(k) number is K252704.

When did F Care RF System (00MEDRF4000US, 05RAFAELOPROBE, 05SPHERAPROBE, 06OUTPUTKAB, 06Pedal1St) receive FDA 510(k) clearance?

F Care RF System (00MEDRF4000US, 05RAFAELOPROBE, 05SPHERAPROBE, 06OUTPUTKAB, 06Pedal1St) received FDA 510(k) clearance on 2025-11-24, under 510(k) number K252704.

Who is the listed applicant for F Care RF System (00MEDRF4000US, 05RAFAELOPROBE, 05SPHERAPROBE, 06OUTPUTKAB, 06Pedal1St)?

The FDA 510(k) record lists F Care Systems USA, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for F Care RF System (00MEDRF4000US, 05RAFAELOPROBE, 05SPHERAPROBE, 06OUTPUTKAB, 06Pedal1St)?

The FDA product code for F Care RF System (00MEDRF4000US, 05RAFAELOPROBE, 05SPHERAPROBE, 06OUTPUTKAB, 06Pedal1St) is GEI.

Essais cliniques associés

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Autres dossiers indiquant F Care Systems USA, LLC en tant que demandeur

K253918Veineo System (00MEDRF4000TCUS 05CR45iT 06Pedal1St)K220725HPR45i K210077MED RF 4000

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Source officielle

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