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FDA 510(k)

ELECTROSTIM I.F.

K-Number: K873566 · 1988-02-01

ApplicantPromatek Industries, Ltd.
Decision Date1988-02-01
Product CodeLIH
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

ELECTROSTIM I.F. is the device name listed in this FDA 510(k) record. The listed applicant is Promatek Industries, Ltd.. It received FDA 510(k) clearance on 1988-02-01 under 510(k) number K873566. 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 ELECTROSTIM I.F.?

ELECTROSTIM I.F. is a medical device that received FDA 510(k) clearance on 1988-02-01. The listed applicant is Promatek Industries, Ltd.. The 510(k) number is K873566.

When did ELECTROSTIM I.F. receive FDA 510(k) clearance?

ELECTROSTIM I.F. received FDA 510(k) clearance on 1988-02-01, under 510(k) number K873566.

Who is the listed applicant for ELECTROSTIM I.F.?

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

What is the FDA product code for ELECTROSTIM I.F.?

The FDA product code for ELECTROSTIM I.F. is LIH.

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.

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Other records listing Promatek Industries, Ltd. 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.

K901417ELECTROSTIM MSTK871472KINESTIM MUSCLE STIMULATOR

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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