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FDA 510(k)

AUTO-TENS MODEL I DISPOS. SINGLE CHAN

K-Number: K823467 · 1983-02-07

ApplicantCbc Corp.
Decision Date1983-02-07
Product CodeGZJ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

AUTO-TENS MODEL I DISPOS. SINGLE CHAN is the device name listed in this FDA 510(k) record. The listed applicant is Cbc Corp.. It received FDA 510(k) clearance on 1983-02-07 under 510(k) number K823467. 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 AUTO-TENS MODEL I DISPOS. SINGLE CHAN?

AUTO-TENS MODEL I DISPOS. SINGLE CHAN is a medical device that received FDA 510(k) clearance on 1983-02-07. The listed applicant is Cbc Corp.. The 510(k) number is K823467.

When did AUTO-TENS MODEL I DISPOS. SINGLE CHAN receive FDA 510(k) clearance?

AUTO-TENS MODEL I DISPOS. SINGLE CHAN received FDA 510(k) clearance on 1983-02-07, under 510(k) number K823467.

Who is the listed applicant for AUTO-TENS MODEL I DISPOS. SINGLE CHAN?

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

What is the FDA product code for AUTO-TENS MODEL I DISPOS. SINGLE CHAN?

The FDA product code for AUTO-TENS MODEL I DISPOS. SINGLE CHAN 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 Cbc Corp. 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.

K832337AUTO-TENS MODEL VK823466AUTO-TENS MODEL III DUAL CHANNEL REPLACEK823465AUTO-TENS MODEL II SINGLE CHANNELK823464AUTO-TENS MODEL IV -DUAL CHANNEL FULL

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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