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FDA 510(k)

RS-4I MUSCLE STIMULATOR FAMILY

K-Number: K032652 · 2003-09-12

ApplicantRs Medical
Decision Date2003-09-12
Product CodeIPF
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

RS-4I MUSCLE STIMULATOR FAMILY is the device name listed in this FDA 510(k) record. The listed applicant is Rs Medical. It received FDA 510(k) clearance on 2003-09-12 under 510(k) number K032652. 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 RS-4I MUSCLE STIMULATOR FAMILY?

RS-4I MUSCLE STIMULATOR FAMILY is a medical device that received FDA 510(k) clearance on 2003-09-12. The listed applicant is Rs Medical. The 510(k) number is K032652.

When did RS-4I MUSCLE STIMULATOR FAMILY receive FDA 510(k) clearance?

RS-4I MUSCLE STIMULATOR FAMILY received FDA 510(k) clearance on 2003-09-12, under 510(k) number K032652.

Who is the listed applicant for RS-4I MUSCLE STIMULATOR FAMILY?

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

What is the FDA product code for RS-4I MUSCLE STIMULATOR FAMILY?

The FDA product code for RS-4I MUSCLE STIMULATOR FAMILY is IPF.

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Other records listing Rs Medical 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.

K112348RS-4I MUSCLE STIMULATORK090951RS- LB LOW BACK CONDUCTIVE GARMENT, MODEL RS-LBM, RS-LBL, RS-FBG FULL BACK CONDUCTIVE GARMENT , MODEL RS-FBGK062325RS-4I MUSCLE STIMULATOR FAMILYK021763RS2MI MUSCLE STIMULATOR FAMILYK000114RS-4M+MUSCLE STIMULATORK990697RS-4V 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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