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FDA 510(k)

STIMTECH NEUROMUSCULAR STIMULATOR, C 600

K-Number: K791048 · 1979-07-03

Decision Date1979-07-03
Product CodeIPF
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

STIMTECH NEUROMUSCULAR STIMULATOR, C 600 is the device name listed in this FDA 510(k) record. The listed applicant is Stimulation Technology, Inc.. It received FDA 510(k) clearance on 1979-07-03 under 510(k) number K791048. The device is classified under product code IPF. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STIMTECH NEUROMUSCULAR STIMULATOR, C 600?

STIMTECH NEUROMUSCULAR STIMULATOR, C 600 is a medical device that received FDA 510(k) clearance on 1979-07-03. The listed applicant is Stimulation Technology, Inc.. The 510(k) number is K791048.

When did STIMTECH NEUROMUSCULAR STIMULATOR, C 600 receive FDA 510(k) clearance?

STIMTECH NEUROMUSCULAR STIMULATOR, C 600 received FDA 510(k) clearance on 1979-07-03, under 510(k) number K791048.

Who is the listed applicant for STIMTECH NEUROMUSCULAR STIMULATOR, C 600?

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

What is the FDA product code for STIMTECH NEUROMUSCULAR STIMULATOR, C 600?

The FDA product code for STIMTECH NEUROMUSCULAR STIMULATOR, C 600 is IPF.

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 Stimulation Technology, 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: IPF)

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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