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FDA 510(k)

MUSCLE STIMULATOR, ELECTRONIC

K-Number: K781139 · 1978-09-26

ApplicantThor Medical Instruments, Inc.
Decision Date1978-09-26
Product CodeIPF
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

MUSCLE STIMULATOR, ELECTRONIC is the device name listed in this FDA 510(k) record. The listed applicant is Thor Medical Instruments, Inc.. It received FDA 510(k) clearance on 1978-09-26 under 510(k) number K781139. 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 MUSCLE STIMULATOR, ELECTRONIC?

MUSCLE STIMULATOR, ELECTRONIC is a medical device that received FDA 510(k) clearance on 1978-09-26. The listed applicant is Thor Medical Instruments, Inc.. The 510(k) number is K781139.

When did MUSCLE STIMULATOR, ELECTRONIC receive FDA 510(k) clearance?

MUSCLE STIMULATOR, ELECTRONIC received FDA 510(k) clearance on 1978-09-26, under 510(k) number K781139.

Who is the listed applicant for MUSCLE STIMULATOR, ELECTRONIC?

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

What is the FDA product code for MUSCLE STIMULATOR, ELECTRONIC?

The FDA product code for MUSCLE STIMULATOR, ELECTRONIC is IPF.

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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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