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FDA 510(k)

MS-189 MUSCLE STIMULATOR

K-Number: K854801 · 1986-03-27

Decision Date1986-03-27
Product CodeIPF
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

MS-189 MUSCLE STIMULATOR is the device name listed in this FDA 510(k) record. The listed applicant is Electro Med Supply, Inc.. It received FDA 510(k) clearance on 1986-03-27 under 510(k) number K854801. 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 MS-189 MUSCLE STIMULATOR?

MS-189 MUSCLE STIMULATOR is a medical device that received FDA 510(k) clearance on 1986-03-27. The listed applicant is Electro Med Supply, Inc.. The 510(k) number is K854801.

When did MS-189 MUSCLE STIMULATOR receive FDA 510(k) clearance?

MS-189 MUSCLE STIMULATOR received FDA 510(k) clearance on 1986-03-27, under 510(k) number K854801.

Who is the listed applicant for MS-189 MUSCLE STIMULATOR?

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

What is the FDA product code for MS-189 MUSCLE STIMULATOR?

The FDA product code for MS-189 MUSCLE STIMULATOR 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 Electro Med Supply, 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.

View all 8 devices →

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

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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