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FDA 510(k)

MULTI-MED MULTI-LUMEN CENTRAL VENOUS CATHETER

K-Number: K955839 · 1996-03-25

ApplicantBaxter Edwards
Decision Date1996-03-25
Product CodeFOZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MULTI-MED MULTI-LUMEN CENTRAL VENOUS CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Baxter Edwards. It received FDA 510(k) clearance on 1996-03-25 under 510(k) number K955839. 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 MULTI-MED MULTI-LUMEN CENTRAL VENOUS CATHETER?

MULTI-MED MULTI-LUMEN CENTRAL VENOUS CATHETER is a medical device that received FDA 510(k) clearance on 1996-03-25. The listed applicant is Baxter Edwards. The 510(k) number is K955839.

When did MULTI-MED MULTI-LUMEN CENTRAL VENOUS CATHETER receive FDA 510(k) clearance?

MULTI-MED MULTI-LUMEN CENTRAL VENOUS CATHETER received FDA 510(k) clearance on 1996-03-25, under 510(k) number K955839.

Who is the listed applicant for MULTI-MED MULTI-LUMEN CENTRAL VENOUS CATHETER?

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

What is the FDA product code for MULTI-MED MULTI-LUMEN CENTRAL VENOUS CATHETER?

The FDA product code for MULTI-MED MULTI-LUMEN CENTRAL VENOUS CATHETER is FOZ.

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Other records listing Baxter Edwards 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.

K993816BAXTER PERCUTANEOUS MECHANICAL THROMBECTOMY (PMT) DEVICE, MODELS PMT0606FD AND PMT1206FDK981909BAXTER HEMOSTASIS VALVE INTRODUCERSK980487CARPENTER-EDWARDS CLASSIC RING WITH DURAFLO TREATMENT MODELS 4425 (MITRAL) AND 4525 (TRICUSPID), CARPENTER-EDWARDS PHYSMK965137FOGARTY VALVULOTOME MODEL 700091K964021INTRAMED SIDE BRANCH OCCLUSION (SBO) SYSTEM (700095 AND 700099)K9526384.5F IMAGECATH CORONARY ANGIOSCOPE, MODEL COV45 [SUBSEQUENTLY REFERRED TO AS THE MODIFIED ANGIOSCOPE[

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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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