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FDA 510(k)

MUSCLE STIMULATOR X-10

K-Number: K840724 · 1984-03-05

ApplicantBiostim, Inc.
Decision Date1984-03-05
Product CodeIPF
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

MUSCLE STIMULATOR X-10 is the device name listed in this FDA 510(k) record. The listed applicant is Biostim, Inc.. It received FDA 510(k) clearance on 1984-03-05 under 510(k) number K840724. 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 X-10?

MUSCLE STIMULATOR X-10 is a medical device that received FDA 510(k) clearance on 1984-03-05. The listed applicant is Biostim, Inc.. The 510(k) number is K840724.

When did MUSCLE STIMULATOR X-10 receive FDA 510(k) clearance?

MUSCLE STIMULATOR X-10 received FDA 510(k) clearance on 1984-03-05, under 510(k) number K840724.

Who is the listed applicant for MUSCLE STIMULATOR X-10?

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

What is the FDA product code for MUSCLE STIMULATOR X-10?

The FDA product code for MUSCLE STIMULATOR X-10 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.

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Other records listing Biostim, 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.

K844023AQUAFORM ELECTRODES WITH AQUAPOREK840725CLINICAL CARE STIMULATORK820678SYSTEM 10K802227ANASTIM II TRANSCUTANEOUS ELECTRICAL

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

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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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