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FDA 510(k)

EP-4 CLINICAL STIMUTATOR

K-Number: K041442 · 2004-09-14

ApplicantEp Medsystems
Decision Date2004-09-14
Product CodeJOQ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

EP-4 CLINICAL STIMUTATOR is the device name listed in this FDA 510(k) record. The listed applicant is Ep Medsystems. It received FDA 510(k) clearance on 2004-09-14 under 510(k) number K041442. The device is classified under product code JOQ. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EP-4 CLINICAL STIMUTATOR?

EP-4 CLINICAL STIMUTATOR is a medical device that received FDA 510(k) clearance on 2004-09-14. The listed applicant is Ep Medsystems. The 510(k) number is K041442.

When did EP-4 CLINICAL STIMUTATOR receive FDA 510(k) clearance?

EP-4 CLINICAL STIMUTATOR received FDA 510(k) clearance on 2004-09-14, under 510(k) number K041442.

Who is the listed applicant for EP-4 CLINICAL STIMUTATOR?

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

What is the FDA product code for EP-4 CLINICAL STIMUTATOR?

The FDA product code for EP-4 CLINICAL STIMUTATOR is JOQ.

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 Ep Medsystems 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.

K092913EP-4TM CARDIAC STIMULATOR, MODELS: EP-04-02, EP-04-04K073709MODIFICATION TO VIEWMATE SYSTEMK071028VIEWMATE SYSTEMK070706EP-WORKMATEK063113EP-WORKMATEK040207EP-4 CLINICAL STIMULATOR

View all 12 devices →

Related Devices (Code: JOQ)

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.

K173439Bloom2 Programmable Electrophysiology StimulatorFischer MedicalK092913EP-4TM CARDIAC STIMULATOR, MODELS: EP-04-02, EP-04-04Ep MedsystemsK072200STIMLABMicropace Pty, Ltd.K070743Z6 STIMULATORSt Cardio Technologies, LLCK040207EP-4 CLINICAL STIMULATOREp MedsystemsK011826EPS320 CARDIAC STIMULATORMicropace Pty, Ltd.

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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