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FDA 510(k)

ELECTRONIC MUSCLE STIMULATOR

K-Number: K811250 · 1981-07-24

ApplicantElectrola
Decision Date1981-07-24
Product CodeIPF
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

ELECTRONIC MUSCLE STIMULATOR is the device name listed in this FDA 510(k) record. The listed applicant is Electrola. It received FDA 510(k) clearance on 1981-07-24 under 510(k) number K811250. The device is classified under product code IPF. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ELECTRONIC MUSCLE STIMULATOR?

ELECTRONIC MUSCLE STIMULATOR is a medical device that received FDA 510(k) clearance on 1981-07-24. The listed applicant is Electrola. The 510(k) number is K811250.

When did ELECTRONIC MUSCLE STIMULATOR receive FDA 510(k) clearance?

ELECTRONIC MUSCLE STIMULATOR received FDA 510(k) clearance on 1981-07-24, under 510(k) number K811250.

Who is the listed applicant for ELECTRONIC MUSCLE STIMULATOR?

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

What is the FDA product code for ELECTRONIC MUSCLE STIMULATOR?

The FDA product code for ELECTRONIC MUSCLE STIMULATOR is IPF.

Related Clinical Trials

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Electrola as applicant

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.

K813181ELECTROC-GYMK810843EPILATRON

Related Devices (Code: IPF)

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.

K253542Apollo Quattro (APQ-10M)Weero Co., Ltd.K252816High Tone Power therapy (HiToP) (Model: HiToP PNP)Mohammadali NezakatiK260142StimelMD (SSMD) systemMotion Informatics ltd.K251083Compact IIEnraf-Nonius, B.V.K241433EVE Synergy (EVE-20M)Weero Co., Ltd.K241488TrainFES AdvanceTrainfes

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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