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FDA 510(k)

VIAPIC CENTRAL LINE CATHETER

K-Number: K860290 · 1986-03-18

ApplicantParke-Davis Co.
Decision Date1986-03-18
Product CodeFOZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

VIAPIC CENTRAL LINE CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Parke-Davis Co.. It received FDA 510(k) clearance on 1986-03-18 under 510(k) number K860290. 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 VIAPIC CENTRAL LINE CATHETER?

VIAPIC CENTRAL LINE CATHETER is a medical device that received FDA 510(k) clearance on 1986-03-18. The listed applicant is Parke-Davis Co.. The 510(k) number is K860290.

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

VIAPIC CENTRAL LINE CATHETER received FDA 510(k) clearance on 1986-03-18, under 510(k) number K860290.

Who is the listed applicant for VIAPIC CENTRAL LINE CATHETER?

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

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

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

Related Clinical Trials

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Other records listing Parke-Davis 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.

K861725INTRACATH INTRAVENOUS CATHETER PLACEMENT UNITK862119DESERET FLO-THRU INJECTATE TEMPERATURE SENSORK855120ATI DISPOSABLE BIOLOGICAL TEST PACKK860570ANGIO-FLO CONTINUOUS ARTERIAL CATH FLUSH DEVICEK852192DISPOSABLE STEAM BIOLOGICAL TEST PACKK841967DESERET THERMODILUTION CARDIAC OUTPUT

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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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