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FDA 510(k)

6F HYDROLYSER THROMBECTOMY CATHETER

K-Number: K990771 · 1999-06-25

ApplicantCordis Corp.
Decision Date1999-06-25
Product CodeQEZ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

6F HYDROLYSER THROMBECTOMY CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Cordis Corp.. It received FDA 510(k) clearance on 1999-06-25 under 510(k) number K990771. The device is classified under product code QEZ. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 6F HYDROLYSER THROMBECTOMY CATHETER?

6F HYDROLYSER THROMBECTOMY CATHETER is a medical device that received FDA 510(k) clearance on 1999-06-25. The listed applicant is Cordis Corp.. The 510(k) number is K990771.

When did 6F HYDROLYSER THROMBECTOMY CATHETER receive FDA 510(k) clearance?

6F HYDROLYSER THROMBECTOMY CATHETER received FDA 510(k) clearance on 1999-06-25, under 510(k) number K990771.

Who is the listed applicant for 6F HYDROLYSER THROMBECTOMY CATHETER?

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 6F HYDROLYSER THROMBECTOMY CATHETER?

The FDA product code for 6F HYDROLYSER THROMBECTOMY CATHETER is QEZ.

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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: QEZ)

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.

K254035Mayumi™ Thrombectomy SystemMicroVention, Inc., d/b/a Terumo NeuroK261105Powered Aventus Thrombectomy System™Inquis MedicalK262030Aventus Thrombectomy SystemInquis MedicalK253589Liberant™ RX Aspiration CatheterMedtronic Interventional Vascular, Inc.K254208FLOWRUNNER Aspiration SystemExpanse Medical, Inc.K253925Aventus Thrombectomy SystemInquis Medical

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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