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FDA 510(k)

CORDIS 9 F GUIDING CATHETER

K-Number: K925131 · 1993-05-06

ApplicantCordis Corp.
Decision Date1993-05-06
Product CodeDQY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CORDIS 9 F GUIDING 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 1993-05-06 under 510(k) number K925131. 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 9 F GUIDING CATHETER?

CORDIS 9 F GUIDING CATHETER is a medical device that received FDA 510(k) clearance on 1993-05-06. The listed applicant is Cordis Corp.. The 510(k) number is K925131.

When did CORDIS 9 F GUIDING CATHETER receive FDA 510(k) clearance?

CORDIS 9 F GUIDING CATHETER received FDA 510(k) clearance on 1993-05-06, under 510(k) number K925131.

Who is the listed applicant for CORDIS 9 F GUIDING 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 9 F GUIDING CATHETER?

The FDA product code for CORDIS 9 F GUIDING CATHETER 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.

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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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