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FDA 510(k)

INTERFERENTIAL STIMULATOR MODEL IMF4150/A

K-Number: K925687 · 1993-03-29

ApplicantBiomedical Life Systems, Inc.
Decision Date1993-03-29
Product CodeLIH
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

INTERFERENTIAL STIMULATOR MODEL IMF4150/A is the device name listed in this FDA 510(k) record. The listed applicant is Biomedical Life Systems, Inc.. It received FDA 510(k) clearance on 1993-03-29 under 510(k) number K925687. 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 STIMULATOR MODEL IMF4150/A?

INTERFERENTIAL STIMULATOR MODEL IMF4150/A is a medical device that received FDA 510(k) clearance on 1993-03-29. The listed applicant is Biomedical Life Systems, Inc.. The 510(k) number is K925687.

When did INTERFERENTIAL STIMULATOR MODEL IMF4150/A receive FDA 510(k) clearance?

INTERFERENTIAL STIMULATOR MODEL IMF4150/A received FDA 510(k) clearance on 1993-03-29, under 510(k) number K925687.

Who is the listed applicant for INTERFERENTIAL STIMULATOR MODEL IMF4150/A?

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

What is the FDA product code for INTERFERENTIAL STIMULATOR MODEL IMF4150/A?

The FDA product code for INTERFERENTIAL STIMULATOR MODEL IMF4150/A is LIH.

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Other records listing Biomedical Life Systems, Inc. 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.

K172971BMLS16-1K102051PAIN BUDDYK061476ELECTRO-NERVE STIMULATOR TENS, MODEL BMLS06-1K042711MODEL BMLS03-7K041388COMBINATION POWERED ELECTRICAL MUSCLE STIMULATOR AND INTERFERENTIAL STIMULATOR, MODEL BMLS04-1K040007INTERFERENTIAL STIMULATOR, MODEL BMLS02-6

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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

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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