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FDA 510(k)

CORDIS ENVOY & VISTA BRITE TIP GUIDING CATHETERS

K-Number: K962362 · 1996-08-08

ApplicantCordis Corp.
Decision Date1996-08-08
Product CodeDQY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CORDIS ENVOY & VISTA BRITE TIP GUIDING CATHETERS is the device name listed in this FDA 510(k) record. The listed applicant is Cordis Corp.. It received FDA 510(k) clearance on 1996-08-08 under 510(k) number K962362. The device is classified under product code DQY. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CORDIS ENVOY & VISTA BRITE TIP GUIDING CATHETERS?

CORDIS ENVOY & VISTA BRITE TIP GUIDING CATHETERS is a medical device that received FDA 510(k) clearance on 1996-08-08. The listed applicant is Cordis Corp.. The 510(k) number is K962362.

When did CORDIS ENVOY & VISTA BRITE TIP GUIDING CATHETERS receive FDA 510(k) clearance?

CORDIS ENVOY & VISTA BRITE TIP GUIDING CATHETERS received FDA 510(k) clearance on 1996-08-08, under 510(k) number K962362.

Who is the listed applicant for CORDIS ENVOY & VISTA BRITE TIP GUIDING CATHETERS?

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 ENVOY & VISTA BRITE TIP GUIDING CATHETERS?

The FDA product code for CORDIS ENVOY & VISTA BRITE TIP GUIDING CATHETERS is DQY.

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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: DQY)

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.

K262817CrossFAST Integrated Microcatheter Advanced Delivery SystemVantis Vascular, Inc.K260559NHanceITIMDS Operation B.V.K262392APRO 35 Swift CatheterAlembic, LLCK262240SSPC NXT Delivery CatheterCenterPoint Systems, LLCK261766CPS Locator 3D Plus Delivery CatheterCenterPoint Systems, LLCK261825Amplatzer TorqVue LP Delivery System; Amplatzer TorqVue LP CatheterAbbott

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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