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FDA 510(k)

TRIPLE LUMEN CENTRAL VENOUS CATHETER

K-Number: K013182 · 2002-07-01

ApplicantCook, Inc.
Decision Date2002-07-01
Product CodeFOZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

TRIPLE LUMEN CENTRAL VENOUS CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Cook, Inc.. It received FDA 510(k) clearance on 2002-07-01 under 510(k) number K013182. The device is classified under product code FOZ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TRIPLE LUMEN CENTRAL VENOUS CATHETER?

TRIPLE LUMEN CENTRAL VENOUS CATHETER is a medical device that received FDA 510(k) clearance on 2002-07-01. The listed applicant is Cook, Inc.. The 510(k) number is K013182.

When did TRIPLE LUMEN CENTRAL VENOUS CATHETER receive FDA 510(k) clearance?

TRIPLE LUMEN CENTRAL VENOUS CATHETER received FDA 510(k) clearance on 2002-07-01, under 510(k) number K013182.

Who is the listed applicant for TRIPLE LUMEN CENTRAL VENOUS CATHETER?

The FDA 510(k) record lists Cook, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TRIPLE LUMEN CENTRAL VENOUS CATHETER?

The FDA product code for TRIPLE LUMEN CENTRAL VENOUS CATHETER is FOZ.

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Other records listing Cook, Inc. 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.

K133634SPECTRUM TURBO-JECT PERIPHERALLY INSERTED CENTRAL VENOUS CATHETER SETK132020ADVANCE 34LP LOW PROFILE PTA BALLOON DILATATION CATHETERK131201ENTUIT SECURE GASTROINTESTIONAL SUTURE ANCHOR SET, ENTUIT SECURE ADJUSTABLE GASTROINTESTINAL SUTURE ANCHOR SETK131206COOK CERVICAL RIPENING BALLOONK132334TURBO-JECT PERIPHERALLY INSERTED CENTRAL VENOUS CATHETER (PICC) SETK122091COOK TURBO-FLO HD ACUTE HEMODIALYSIS CATHETER SET/TRAY COOK SPECTRUM TURBO-FLO HD ACUTE HEMODIALYSIS CATHETER SET/TRAY

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Related Devices (Code: FOZ)

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.

K260432Ruby Intravascular CatheterVenocare, Inc.K260165Unimpregnated Central Venous CatheterSpectrum VascularK261041ClearSafe Closed SystemMedSource Labs, LLCK260539MedSource QuickSafe™ Safety IV Catheter; MedSource PurSafe™ Safety IV CatheterMedSource Labs, LLCK253235Introcan Safety® Deep Access XL IV CatheterB.Braun Medical, Inc.K252137BD Insyte™ IV CatheterBecton Dickinson Infusion Therapy Systems, Inc.

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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