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FDA 510(k)

ELECTROSTIM MST

K-Number: K901417 · 1990-08-28

ApplicantPromatek Industries, Ltd.
Decision Date1990-08-28
Product CodeGZJ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

ELECTROSTIM MST 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 1990-08-28 under 510(k) number K901417. The device is classified under product code GZJ. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ELECTROSTIM MST?

ELECTROSTIM MST is a medical device that received FDA 510(k) clearance on 1990-08-28. The listed applicant is Promatek Industries, Ltd.. The 510(k) number is K901417.

When did ELECTROSTIM MST receive FDA 510(k) clearance?

ELECTROSTIM MST received FDA 510(k) clearance on 1990-08-28, under 510(k) number K901417.

Who is the listed applicant for ELECTROSTIM MST?

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 MST?

The FDA product code for ELECTROSTIM MST is GZJ.

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.

K873566ELECTROSTIM I.F.K871472KINESTIM MUSCLE STIMULATOR

Related Devices (Code: GZJ)

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.

K252712STIMPOD NMS460 Nerve StimulatorAlgiamed Technologies USA, Inc.K252767actiTENS miniSublimedK252236CP Relief Wand Rx - TENS/NMESN & C Holdings, LLCK232441Unipro (K-UNIPRO-US)Tenscare, Ltd.K241228TENSWaveZynex Medical OfficerK233046Electrical Neuromuscular Stimulator, Cure TrioOriental Inspiration Limited

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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