Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

RS2MI MUSCLE STIMULATOR FAMILY

K-Number: K021763 · 2002-06-13

ApplicantRs Medical
Decision Date2002-06-13
Product CodeIPF
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

RS2MI 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 2002-06-13 under 510(k) number K021763. 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 RS2MI MUSCLE STIMULATOR FAMILY?

RS2MI MUSCLE STIMULATOR FAMILY is a medical device that received FDA 510(k) clearance on 2002-06-13. The listed applicant is Rs Medical. The 510(k) number is K021763.

When did RS2MI MUSCLE STIMULATOR FAMILY receive FDA 510(k) clearance?

RS2MI MUSCLE STIMULATOR FAMILY received FDA 510(k) clearance on 2002-06-13, under 510(k) number K021763.

Who is the listed applicant for RS2MI 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 RS2MI MUSCLE STIMULATOR FAMILY?

The FDA product code for RS2MI MUSCLE STIMULATOR FAMILY 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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

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 FAMILYK032652RS-4I MUSCLE STIMULATOR FAMILYK000114RS-4M+MUSCLE STIMULATORK990697RS-4V MUSCLE STIMULATOR

View all 10 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.

↑