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FDA 510(k)

MULTILUMEN VIAPIC CENTRAL LINE CATHETER

K-Number: K861510 · 1986-06-09

ApplicantWarner-Lambert Co.
Decision Date1986-06-09
Product CodeFOZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MULTILUMEN VIAPIC CENTRAL LINE CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Warner-Lambert Co.. It received FDA 510(k) clearance on 1986-06-09 under 510(k) number K861510. 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 MULTILUMEN VIAPIC CENTRAL LINE CATHETER?

MULTILUMEN VIAPIC CENTRAL LINE CATHETER is a medical device that received FDA 510(k) clearance on 1986-06-09. The listed applicant is Warner-Lambert Co.. The 510(k) number is K861510.

When did MULTILUMEN VIAPIC CENTRAL LINE CATHETER receive FDA 510(k) clearance?

MULTILUMEN VIAPIC CENTRAL LINE CATHETER received FDA 510(k) clearance on 1986-06-09, under 510(k) number K861510.

Who is the listed applicant for MULTILUMEN VIAPIC CENTRAL LINE CATHETER?

The FDA 510(k) record lists Warner-Lambert Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MULTILUMEN VIAPIC CENTRAL LINE CATHETER?

The FDA product code for MULTILUMEN VIAPIC CENTRAL LINE CATHETER is FOZ.

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Other records listing Warner-Lambert Co. 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.

K024160NEOSPORIN SCAR SOLUTIONK893452EXTRA STRENGTH EFFERGRIP DENTURE ADHESIVE CREAMK870584O.P.T.(TM) OVULATION PREDICTION TESTK852967GENERAL DIAGNOSTICS' CEFTRIAXONE 30MCG SUSDEP DISKK852689GENERAL DIAGNOSTICS CEFTAZIDIME 30 MCG SUSC DISKK852843GENERAL DIAGNOSTICS COAG-A-MATE XC

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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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