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FDA 510(k)

TENS-IT

K-Number: K933368 · 1994-06-07

ApplicantElectro Med Supply, Inc.
Decision Date1994-06-07
Product CodeGZJ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

TENS-IT is the device name listed in this FDA 510(k) record. The listed applicant is Electro Med Supply, Inc.. It received FDA 510(k) clearance on 1994-06-07 under 510(k) number K933368. 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 TENS-IT?

TENS-IT is a medical device that received FDA 510(k) clearance on 1994-06-07. The listed applicant is Electro Med Supply, Inc.. The 510(k) number is K933368.

When did TENS-IT receive FDA 510(k) clearance?

TENS-IT received FDA 510(k) clearance on 1994-06-07, under 510(k) number K933368.

Who is the listed applicant for TENS-IT?

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

What is the FDA product code for TENS-IT?

The FDA product code for TENS-IT is GZJ.

Other records listing Electro Med Supply, 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.

K872208MS-112, POWERED MUSCLE STIMULATORK872207MS-108, POWERED MUSCLE STIMULATORK872206MD-104, POWERED MUSCLE STIMULATORK862487MS-139 ELECTRONIC MUSCLE STIMULATORK862485MS-179 ELECTRONIC MUSCLE STIMULATORK862486MS-159 ELECTRONIC MUSCLE STIMULATOR

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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

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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