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FDA 510(k)

CORDIS ELECTROPHYSIOLOGY STIMULATOR

K-Number: K844815 · 1985-06-11

ApplicantCordis Corp.
Decision Date1985-06-11
Product CodeJOQ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CORDIS ELECTROPHYSIOLOGY STIMULATOR is the device name listed in this FDA 510(k) record. The listed applicant is Cordis Corp.. It received FDA 510(k) clearance on 1985-06-11 under 510(k) number K844815. 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 CORDIS ELECTROPHYSIOLOGY STIMULATOR?

CORDIS ELECTROPHYSIOLOGY STIMULATOR is a medical device that received FDA 510(k) clearance on 1985-06-11. The listed applicant is Cordis Corp.. The 510(k) number is K844815.

When did CORDIS ELECTROPHYSIOLOGY STIMULATOR receive FDA 510(k) clearance?

CORDIS ELECTROPHYSIOLOGY STIMULATOR received FDA 510(k) clearance on 1985-06-11, under 510(k) number K844815.

Who is the listed applicant for CORDIS ELECTROPHYSIOLOGY STIMULATOR?

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

What is the FDA product code for CORDIS ELECTROPHYSIOLOGY STIMULATOR?

The FDA product code for CORDIS ELECTROPHYSIOLOGY STIMULATOR is JOQ.

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Other records listing Cordis 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.

K112797POWERFLEX PRO PERCUTANEOUS TRANSLUMINAL ANGIOPLASTY CATHETERK101651ANGIOGUARD XP EMBOLI CAPTURE GUIDEWIRE, ANGIOGUARD RX EMBOLI CAPTURE GUIDEWIREK082143MICRO GUIDE CATHETER XPK062798SMART NITINOL SELF-EXPANDING STENT, MODEL C06120MB, C07120MB, C08120MB, C06150MB, C07150MB, C08150MBK060877PALMAZ BLUE .014 TRANSHEPATIC BILIARY STENT SYSTEM-MODEL PB1550,BAS,BAX,PB1560,BAS,BAX,PB1850,BAS,BAXPB1860BAS,BAXK050645CORDIS AMIIA .014 PTA BALLOON CATHETER

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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, LLCK041442EP-4 CLINICAL STIMUTATOREp MedsystemsK040207EP-4 CLINICAL STIMULATOREp Medsystems

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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