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FDA 510(k)

CODETRON TRANSCUTANEOUS ELECTRICAL NERVE STIMULA.

K-Number: K863469 · 1987-02-20

ApplicantCordis Corp.
Decision Date1987-02-20
Product CodeGZJ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

CODETRON TRANSCUTANEOUS ELECTRICAL NERVE STIMULA. is the device name listed in this FDA 510(k) record. The listed applicant is Cordis Corp.. It received FDA 510(k) clearance on 1987-02-20 under 510(k) number K863469. The device is classified under product code GZJ. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CODETRON TRANSCUTANEOUS ELECTRICAL NERVE STIMULA.?

CODETRON TRANSCUTANEOUS ELECTRICAL NERVE STIMULA. is a medical device that received FDA 510(k) clearance on 1987-02-20. The listed applicant is Cordis Corp.. The 510(k) number is K863469.

When did CODETRON TRANSCUTANEOUS ELECTRICAL NERVE STIMULA. receive FDA 510(k) clearance?

CODETRON TRANSCUTANEOUS ELECTRICAL NERVE STIMULA. received FDA 510(k) clearance on 1987-02-20, under 510(k) number K863469.

Who is the listed applicant for CODETRON TRANSCUTANEOUS ELECTRICAL NERVE STIMULA.?

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 CODETRON TRANSCUTANEOUS ELECTRICAL NERVE STIMULA.?

The FDA product code for CODETRON TRANSCUTANEOUS ELECTRICAL NERVE STIMULA. is GZJ.

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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: GZJ)

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.

K252712STIMPOD NMS460 Nerve StimulatorAlgiamed Technologies USA, Inc.K252767actiTENS miniSublimedK252236CP Relief Wand Rx - TENS/NMESN & C Holdings, LLCK232441Unipro (K-UNIPRO-US)Tenscare, Ltd.K241228TENSWaveZynex Medical OfficerK233046Electrical Neuromuscular Stimulator, Cure TrioOriental Inspiration Limited

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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