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FDA 510(k)

SELECTRODE SYSTEM

K-Number: K832634 · 1984-01-25

ApplicantBio-Stimu Trend Corp.
Decision Date1984-01-25
Product CodeBWK
DecisionSubstantially Equivalent

Device Summary

SELECTRODE SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Bio-Stimu Trend Corp.. It received FDA 510(k) clearance on 1984-01-25 under 510(k) number K832634. The device is classified under product code BWK. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SELECTRODE SYSTEM?

SELECTRODE SYSTEM is a medical device that received FDA 510(k) clearance on 1984-01-25. The listed applicant is Bio-Stimu Trend Corp.. The 510(k) number is K832634.

When did SELECTRODE SYSTEM receive FDA 510(k) clearance?

SELECTRODE SYSTEM received FDA 510(k) clearance on 1984-01-25, under 510(k) number K832634.

Who is the listed applicant for SELECTRODE SYSTEM?

The FDA 510(k) record lists Bio-Stimu Trend Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SELECTRODE SYSTEM?

The FDA product code for SELECTRODE SYSTEM is BWK.

Related Clinical Trials

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Other records listing Bio-Stimu Trend Corp. 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.

K842033ELECTRODE PLACEMENT ARM PART GARMENTK840591ELECTRODE PLACEMENT SLEEVEK840592ELECTRODE PLACEMENT LUMBAR SHORTS

Related Devices (Code: BWK)

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.

K244030Needle Stimulator (CMNS6-1 PLUS, CMNS6-3)Wuxi Jiajian Medical Instrument Co., Ltd.K220153Needle Stimulator (Model: RJNS6-1)Bozhou Rongjian Medical Appliance Co., Ltd.K202861Needle StimulatorWuxi Jiajian Medical Instrument Co., Ltd.K200636AXUS ES-5 Electro-Acupuncture DeviceLhasa Oms, Inc.K170391ANSiStim-PPDyansys, Inc.K152571StivaxBiegler GmbH

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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