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FDA 510(k)

MS-112, POWERED MUSCLE STIMULATOR

K-Number: K872208 · 1987-10-06

ApplicantElectro Med Supply, Inc.
Decision Date1987-10-06
Product CodeIPF
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

MS-112, POWERED 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 1987-10-06 under 510(k) number K872208. 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-112, POWERED MUSCLE STIMULATOR?

MS-112, POWERED MUSCLE STIMULATOR is a medical device that received FDA 510(k) clearance on 1987-10-06. The listed applicant is Electro Med Supply, Inc.. The 510(k) number is K872208.

When did MS-112, POWERED MUSCLE STIMULATOR receive FDA 510(k) clearance?

MS-112, POWERED MUSCLE STIMULATOR received FDA 510(k) clearance on 1987-10-06, under 510(k) number K872208.

Who is the listed applicant for MS-112, POWERED 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-112, POWERED MUSCLE STIMULATOR?

The FDA product code for MS-112, POWERED MUSCLE STIMULATOR is IPF.

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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.

K933368TENS-ITK872207MS-108, POWERED MUSCLE STIMULATORK872206MD-104, POWERED MUSCLE STIMULATORK862487MS-139 ELECTRONIC MUSCLE STIMULATORK862485MS-179 ELECTRONIC MUSCLE STIMULATORK862486MS-159 ELECTRONIC MUSCLE STIMULATOR

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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.

K253542Apollo Quattro (APQ-10M)Weero Co., Ltd.K252816High Tone Power therapy (HiToP) (Model: HiToP PNP)Mohammadali NezakatiK260142StimelMD (SSMD) systemMotion Informatics ltd.K251083Compact IIEnraf-Nonius, B.V.K241433EVE Synergy (EVE-20M)Weero Co., Ltd.K241488TrainFES AdvanceTrainfes

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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