FDA 510(k)

MYO-STIM

K-Number: K781239 · 1978-11-03

Decision Date1978-11-03

Product CodeIPF

Advisory CommitteePM

DecisionSubstantially Equivalent

Device Summary

MYO-STIM is the device name listed in this FDA 510(k) record. The listed applicant is Med General. It received FDA 510(k) clearance on 1978-11-03 under 510(k) number K781239. 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 MYO-STIM?

MYO-STIM is a medical device that received FDA 510(k) clearance on 1978-11-03. The listed applicant is Med General. The 510(k) number is K781239.

When did MYO-STIM receive FDA 510(k) clearance?

MYO-STIM received FDA 510(k) clearance on 1978-11-03, under 510(k) number K781239.

Who is the listed applicant for MYO-STIM?

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

What is the FDA product code for MYO-STIM?

The FDA product code for MYO-STIM is IPF.

Other records listing Med General 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.

K791097CEPTORTRODE WITH CEPTOR HESIVE K791098SINGLE-USE MINI-BULLDOG K790763MAXI-VAC TM K790269CEPTOR HESIVE K782006MEDGENERAL SINGLE-USE BULLDOG K780632MAXICEPTOR

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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.