FDA 510(k)

INTERFERENTIAL CURRENT THERAPY UNIT

K-Number: K931768 · 1994-02-23

Decision Date1994-02-23

Product CodeLIH

Advisory CommitteeNE

DecisionSubstantially Equivalent

Device Summary

INTERFERENTIAL CURRENT THERAPY UNIT is the device name listed in this FDA 510(k) record. The listed applicant is Lumiscope Co., Inc.. It received FDA 510(k) clearance on 1994-02-23 under 510(k) number K931768. 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 THERAPY UNIT?

INTERFERENTIAL CURRENT THERAPY UNIT is a medical device that received FDA 510(k) clearance on 1994-02-23. The listed applicant is Lumiscope Co., Inc.. The 510(k) number is K931768.

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

INTERFERENTIAL CURRENT THERAPY UNIT received FDA 510(k) clearance on 1994-02-23, under 510(k) number K931768.

Who is the listed applicant for INTERFERENTIAL CURRENT THERAPY UNIT?

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

What is the FDA product code for INTERFERENTIAL CURRENT THERAPY UNIT?

The FDA product code for INTERFERENTIAL CURRENT THERAPY UNIT is LIH.

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Other records listing Lumiscope Co., Inc. as applicant

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Related Devices (Code: LIH)

K231575Vecttor VT-300Artaflex, Inc.K202725ETD4000Therasigma, LLC K183692Avid IF2Vision Quest Industries Inc./Dba VQ Orthocare K122944GEMORE TRUE SINE INTERFERENTIAL STIMULATORGemore Technology Co, Ltd.K121662VECTTOR VT-200Alan Neuromedical Technologies, LLC K110509EVERYWAY INTERFERNTIAL STIMULATOR, MODEL IF-908Everyway Medical Instruments Co.,Ltd

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.