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FDA 510(k)

DENDRITE VM-TRANSCUTANEOUS ELEC. NERVE

K-Number: K823002 · 1982-11-17

ApplicantTri W-G, Inc.
Decision Date1982-11-17
Product CodeGZJ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

DENDRITE VM-TRANSCUTANEOUS ELEC. NERVE is the device name listed in this FDA 510(k) record. The listed applicant is Tri W-G, Inc.. It received FDA 510(k) clearance on 1982-11-17 under 510(k) number K823002. 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 DENDRITE VM-TRANSCUTANEOUS ELEC. NERVE?

DENDRITE VM-TRANSCUTANEOUS ELEC. NERVE is a medical device that received FDA 510(k) clearance on 1982-11-17. The listed applicant is Tri W-G, Inc.. The 510(k) number is K823002.

When did DENDRITE VM-TRANSCUTANEOUS ELEC. NERVE receive FDA 510(k) clearance?

DENDRITE VM-TRANSCUTANEOUS ELEC. NERVE received FDA 510(k) clearance on 1982-11-17, under 510(k) number K823002.

Who is the listed applicant for DENDRITE VM-TRANSCUTANEOUS ELEC. NERVE?

The FDA 510(k) record lists Tri W-G, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DENDRITE VM-TRANSCUTANEOUS ELEC. NERVE?

The FDA product code for DENDRITE VM-TRANSCUTANEOUS ELEC. NERVE is GZJ.

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Other records listing Tri W-G, 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.

K960196TRI W-G, INC TABLE, TILT/EXAM/TREATMENT MODEL 777K945163ECHOCARDIOGRAPHYK941720MODEL 747 AND 747-30 EXAM/TREATMENT TABLEK936303TREATMENT TABLE MODIFICATIONK933119HI-LO TREATMENT TABLESK932746MODEL T4501,T4502,T4503,T4504,T4504 TILT TABLE

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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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