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FDA 510(k)

CORDIS ANGIOPLASTY HEMOSTASIS DEVICES

K-Number: K863177 · 1986-10-15

ApplicantCordis Corp.
Decision Date1986-10-15
Product CodeDTL
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CORDIS ANGIOPLASTY HEMOSTASIS DEVICES is the device name listed in this FDA 510(k) record. The listed applicant is Cordis Corp.. It received FDA 510(k) clearance on 1986-10-15 under 510(k) number K863177. The device is classified under product code DTL. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CORDIS ANGIOPLASTY HEMOSTASIS DEVICES?

CORDIS ANGIOPLASTY HEMOSTASIS DEVICES is a medical device that received FDA 510(k) clearance on 1986-10-15. The listed applicant is Cordis Corp.. The 510(k) number is K863177.

When did CORDIS ANGIOPLASTY HEMOSTASIS DEVICES receive FDA 510(k) clearance?

CORDIS ANGIOPLASTY HEMOSTASIS DEVICES received FDA 510(k) clearance on 1986-10-15, under 510(k) number K863177.

Who is the listed applicant for CORDIS ANGIOPLASTY HEMOSTASIS DEVICES?

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 ANGIOPLASTY HEMOSTASIS DEVICES?

The FDA product code for CORDIS ANGIOPLASTY HEMOSTASIS DEVICES is DTL.

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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: DTL)

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.

K131124COLIGNJilin Coronado Medical , Ltd.K123448AFFINITY FLEXIBLE LUER LOCK ADAPTER WITH BALANCE BIOSURFACE, AFFINITY FLEXIBLE LUER LOCK ADAPTER WITH CARMEDA BIOACTIVEMedtronic, Inc.K122811CONNECTOR COMPONENTS WITH BALANCE BIOSURFACEMedtronic, Inc.K122301GUARDIAN II HEMOSTASIS VALVE GUARDIAN II NC HEMOSTASIS VALVEVascular Solutions Zerusa , Ltd.K120069MEDLINE STOPCOCK AND MANIFOLDMedline Industries, Inc.K113148E-PASSSynexmed(Shenzhen)Company 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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