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FDA 510(k)

STIMULATOR, ELECTRICAL NERVE

K-Number: K782127 · 1979-01-05

Decision Date1979-01-05
Product CodeGZJ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

STIMULATOR, ELECTRICAL NERVE is the device name listed in this FDA 510(k) record. The listed applicant is Somatronics, Inc.. It received FDA 510(k) clearance on 1979-01-05 under 510(k) number K782127. 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 STIMULATOR, ELECTRICAL NERVE?

STIMULATOR, ELECTRICAL NERVE is a medical device that received FDA 510(k) clearance on 1979-01-05. The listed applicant is Somatronics, Inc.. The 510(k) number is K782127.

When did STIMULATOR, ELECTRICAL NERVE receive FDA 510(k) clearance?

STIMULATOR, ELECTRICAL NERVE received FDA 510(k) clearance on 1979-01-05, under 510(k) number K782127.

Who is the listed applicant for STIMULATOR, ELECTRICAL NERVE?

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

What is the FDA product code for STIMULATOR, ELECTRICAL NERVE?

The FDA product code for STIMULATOR, ELECTRICAL NERVE 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.

Other records listing Somatronics, 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.

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.

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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