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FDA 510(k)

DESERET INFANT CENTRAL VENOUS CATHE-

K-Number: K840116 · 1984-03-22

ApplicantParke-Davis Co.
Decision Date1984-03-22
Product CodeFOZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

DESERET INFANT CENTRAL VENOUS CATHE- 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 1984-03-22 under 510(k) number K840116. 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 DESERET INFANT CENTRAL VENOUS CATHE-?

DESERET INFANT CENTRAL VENOUS CATHE- is a medical device that received FDA 510(k) clearance on 1984-03-22. The listed applicant is Parke-Davis Co.. The 510(k) number is K840116.

When did DESERET INFANT CENTRAL VENOUS CATHE- receive FDA 510(k) clearance?

DESERET INFANT CENTRAL VENOUS CATHE- received FDA 510(k) clearance on 1984-03-22, under 510(k) number K840116.

Who is the listed applicant for DESERET INFANT CENTRAL VENOUS CATHE-?

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 DESERET INFANT CENTRAL VENOUS CATHE-?

The FDA product code for DESERET INFANT CENTRAL VENOUS CATHE- is FOZ.

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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 DEVICEK860290VIAPIC CENTRAL LINE CATHETERK852192DISPOSABLE STEAM BIOLOGICAL TEST PACK

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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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