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FDA 510(k)

STIMULATOR, MUSCLE, MODEL 107

K-Number: K770725 · 1977-04-26

ApplicantJaytronics, Inc.
Decision Date1977-04-26
Product CodeGZI
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

STIMULATOR, MUSCLE, MODEL 107 is the device name listed in this FDA 510(k) record. The listed applicant is Jaytronics, Inc.. It received FDA 510(k) clearance on 1977-04-26 under 510(k) number K770725. The device is classified under product code GZI. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STIMULATOR, MUSCLE, MODEL 107?

STIMULATOR, MUSCLE, MODEL 107 is a medical device that received FDA 510(k) clearance on 1977-04-26. The listed applicant is Jaytronics, Inc.. The 510(k) number is K770725.

When did STIMULATOR, MUSCLE, MODEL 107 receive FDA 510(k) clearance?

STIMULATOR, MUSCLE, MODEL 107 received FDA 510(k) clearance on 1977-04-26, under 510(k) number K770725.

Who is the listed applicant for STIMULATOR, MUSCLE, MODEL 107?

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

What is the FDA product code for STIMULATOR, MUSCLE, MODEL 107?

The FDA product code for STIMULATOR, MUSCLE, MODEL 107 is GZI.

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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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