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FDA 510(k)

CORDIS MAXI LD LARGE DIAMETER BALLOON DILATATION CATHETER

K-Number: K993720 · 2000-01-18

ApplicantCordis Corp.
Decision Date2000-01-18
Product CodeKNQ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

CORDIS MAXI LD LARGE DIAMETER BALLOON DILATATION 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 2000-01-18 under 510(k) number K993720. The device is classified under product code KNQ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CORDIS MAXI LD LARGE DIAMETER BALLOON DILATATION CATHETER?

CORDIS MAXI LD LARGE DIAMETER BALLOON DILATATION CATHETER is a medical device that received FDA 510(k) clearance on 2000-01-18. The listed applicant is Cordis Corp.. The 510(k) number is K993720.

When did CORDIS MAXI LD LARGE DIAMETER BALLOON DILATATION CATHETER receive FDA 510(k) clearance?

CORDIS MAXI LD LARGE DIAMETER BALLOON DILATATION CATHETER received FDA 510(k) clearance on 2000-01-18, under 510(k) number K993720.

Who is the listed applicant for CORDIS MAXI LD LARGE DIAMETER BALLOON DILATATION 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 CORDIS MAXI LD LARGE DIAMETER BALLOON DILATATION CATHETER?

The FDA product code for CORDIS MAXI LD LARGE DIAMETER BALLOON DILATATION CATHETER is KNQ.

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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: KNQ)

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.

K122924CRE FIXED WIRE BALLON DILATION CATHETERBoston Scientific CorpK093236ETHICON ENDO-SURGERYOPTICAL DILATOREthicon Endo-Surgery, Inc.K090183HERCULES 3 STAGE WIRE GUIDED DILATION BALLOONCook EndoscopyK082995SMART DILATORSafestitch MedicalK061937COOK ENDOSCOPY ESOPHAGEAL DILATION BALLOONCook EndoscopyK061787MAXFORCE TTS SINGLE-USE BALLOON DILATORBoston Scientific Corp

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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