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FDA 510(k)

INTERFERENTIAL CURRENT UNIT

K-Number: K874119 · 1988-01-22

ApplicantCompustim Electronics
Decision Date1988-01-22
Product CodeLIH
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

INTERFERENTIAL CURRENT UNIT is the device name listed in this FDA 510(k) record. The listed applicant is Compustim Electronics. It received FDA 510(k) clearance on 1988-01-22 under 510(k) number K874119. The device is classified under product code LIH. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INTERFERENTIAL CURRENT UNIT?

INTERFERENTIAL CURRENT UNIT is a medical device that received FDA 510(k) clearance on 1988-01-22. The listed applicant is Compustim Electronics. The 510(k) number is K874119.

When did INTERFERENTIAL CURRENT UNIT receive FDA 510(k) clearance?

INTERFERENTIAL CURRENT UNIT received FDA 510(k) clearance on 1988-01-22, under 510(k) number K874119.

Who is the listed applicant for INTERFERENTIAL CURRENT UNIT?

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

What is the FDA product code for INTERFERENTIAL CURRENT UNIT?

The FDA product code for INTERFERENTIAL CURRENT UNIT is LIH.

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Related Devices (Code: LIH)

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.

K231575Vecttor VT-300Artaflex, Inc.K202725ETD4000Therasigma, LLCK183692Avid IF2Vision Quest Industries Inc./Dba VQ OrthocareK122944GEMORE TRUE SINE INTERFERENTIAL STIMULATORGemore Technology Co, Ltd.K121662VECTTOR VT-200Alan Neuromedical Technologies, LLCK110509EVERYWAY INTERFERNTIAL STIMULATOR, MODEL IF-908Everyway Medical Instruments Co.,Ltd

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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