FDA 510(k)

STIMPOD NMS460 Nerve Stimulator

Numéro K : K252712 · 2026-05-28

DemandeurAlgiamed Technologies USA, Inc.

Date de décision2026-05-28

Code produitGZJ

Comité consultatifNE

DécisionSubstantially Equivalent

Résumé du dispositif

STIMPOD NMS460 Nerve Stimulator is the device name listed in this FDA 510(k) record. The listed applicant is Algiamed Technologies USA, Inc.. It received FDA 510(k) clearance on 2026-05-28 under 510(k) number K252712. The device is classified under product code GZJ. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Questions fréquentes

What is the STIMPOD NMS460 Nerve Stimulator?

STIMPOD NMS460 Nerve Stimulator is a medical device that received FDA 510(k) clearance on 2026-05-28. The listed applicant is Algiamed Technologies USA, Inc.. The 510(k) number is K252712.

When did STIMPOD NMS460 Nerve Stimulator receive FDA 510(k) clearance?

STIMPOD NMS460 Nerve Stimulator received FDA 510(k) clearance on 2026-05-28, under 510(k) number K252712.

Who is the listed applicant for STIMPOD NMS460 Nerve Stimulator?

The FDA 510(k) record lists Algiamed Technologies USA, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for STIMPOD NMS460 Nerve Stimulator?

The FDA product code for STIMPOD NMS460 Nerve Stimulator is GZJ.

Essais cliniques associés

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Dispositifs connexes (Code : GZJ)

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Source officielle

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