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FDA 510(k)

MUSCLE STIMULATOR, ELECTRICAL

K-Number: K781113 · 1978-09-26

ApplicantRich-Mar Corp.
Decision Date1978-09-26
Product CodeIPF
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

MUSCLE STIMULATOR, ELECTRICAL is the device name listed in this FDA 510(k) record. The listed applicant is Rich-Mar Corp.. It received FDA 510(k) clearance on 1978-09-26 under 510(k) number K781113. 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, ELECTRICAL?

MUSCLE STIMULATOR, ELECTRICAL is a medical device that received FDA 510(k) clearance on 1978-09-26. The listed applicant is Rich-Mar Corp.. The 510(k) number is K781113.

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

MUSCLE STIMULATOR, ELECTRICAL received FDA 510(k) clearance on 1978-09-26, under 510(k) number K781113.

Who is the listed applicant for MUSCLE STIMULATOR, ELECTRICAL?

The FDA 510(k) record lists Rich-Mar Corp. as the applicant. This does not by itself establish the device manufacturer.

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

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

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Other records listing Rich-Mar Corp. 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.

K040679RICH-MAR AUTOPRISM INFRARED LAMPK031018AUTOGEL PADK032941AUTOSOUND 7.6 MUSCLE STIMULATOR, TENS, THERAPEUTIC ULTRASOUND AND COMBINATION DEVICEK021483RICH-MAR THERASOUND 6.5 THERAPEUTIC ULTRASOUNDK013770MODIFICATION TO: WINNER ST-2 STIMULATORK013771MODIFICATION TO: WINNER CM-2 MUSCLE STIMULATOR, TENS, THERAPEUTIC ULTRASOUND AND COMBINATION DEVICE

View all 43 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.

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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