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FDA 510(k)

ZIMMER TENS

K-Number: K894388 · 1989-08-10

ApplicantAmerican Imex
Decision Date1989-08-10
Product CodeGZJ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

ZIMMER TENS is the device name listed in this FDA 510(k) record. The listed applicant is American Imex. It received FDA 510(k) clearance on 1989-08-10 under 510(k) number K894388. 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 ZIMMER TENS?

ZIMMER TENS is a medical device that received FDA 510(k) clearance on 1989-08-10. The listed applicant is American Imex. The 510(k) number is K894388.

When did ZIMMER TENS receive FDA 510(k) clearance?

ZIMMER TENS received FDA 510(k) clearance on 1989-08-10, under 510(k) number K894388.

Who is the listed applicant for ZIMMER TENS?

The FDA 510(k) record lists American Imex as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ZIMMER TENS?

The FDA product code for ZIMMER TENS is GZJ.

Related Clinical Trials

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Other records listing American Imex 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.

K032003PREMIER PLUSK982221PREMIER APK926326MICROCARE(TM)K912289ULTIMA XS, MODIFICATIONK895295ULTIMA XS MICROCURRENT TENSK881704EASY TENS

View all 11 devices →

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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