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FDA 510(k)

ANODYNE II-ELECTRICAL NEURO STIMULATOR

K-Number: K761053 · 1976-11-30

ApplicantRich-Mar Corp.
Decision Date1976-11-30
Product CodeGZJ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

ANODYNE II-ELECTRICAL NEURO STIMULATOR is the device name listed in this FDA 510(k) record. The listed applicant is Rich-Mar Corp.. It received FDA 510(k) clearance on 1976-11-30 under 510(k) number K761053. 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 ANODYNE II-ELECTRICAL NEURO STIMULATOR?

ANODYNE II-ELECTRICAL NEURO STIMULATOR is a medical device that received FDA 510(k) clearance on 1976-11-30. The listed applicant is Rich-Mar Corp.. The 510(k) number is K761053.

When did ANODYNE II-ELECTRICAL NEURO STIMULATOR receive FDA 510(k) clearance?

ANODYNE II-ELECTRICAL NEURO STIMULATOR received FDA 510(k) clearance on 1976-11-30, under 510(k) number K761053.

Who is the listed applicant for ANODYNE II-ELECTRICAL NEURO STIMULATOR?

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

What is the FDA product code for ANODYNE II-ELECTRICAL NEURO STIMULATOR?

The FDA product code for ANODYNE II-ELECTRICAL NEURO STIMULATOR is GZJ.

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Other records listing Rich-Mar 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.

K040679RICH-MAR AUTOPRISM INFRARED LAMPK031018AUTOGEL PADK032941AUTOSOUND 7.6 MUSCLE STIMULATOR, TENS, THERAPEUTIC ULTRASOUND AND COMBINATION DEVICEK021483RICH-MAR THERASOUND 6.5 THERAPEUTIC ULTRASOUNDK013770MODIFICATION TO: WINNER ST-2 STIMULATORK013771MODIFICATION TO: WINNER CM-2 MUSCLE STIMULATOR, TENS, THERAPEUTIC ULTRASOUND AND COMBINATION DEVICE

View all 43 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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