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FDA 510(k)

MULTIPLE I.V. SETS

K-Number: K854804 · 1986-02-12

ApplicantC. B. Dumont Company, Inc.
Decision Date1986-02-12
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MULTIPLE I.V. SETS is the device name listed in this FDA 510(k) record. The listed applicant is C. B. Dumont Company, Inc.. It received FDA 510(k) clearance on 1986-02-12 under 510(k) number K854804. The device is classified under product code FPA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MULTIPLE I.V. SETS?

MULTIPLE I.V. SETS is a medical device that received FDA 510(k) clearance on 1986-02-12. The listed applicant is C. B. Dumont Company, Inc.. The 510(k) number is K854804.

When did MULTIPLE I.V. SETS receive FDA 510(k) clearance?

MULTIPLE I.V. SETS received FDA 510(k) clearance on 1986-02-12, under 510(k) number K854804.

Who is the listed applicant for MULTIPLE I.V. SETS?

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

What is the FDA product code for MULTIPLE I.V. SETS?

The FDA product code for MULTIPLE I.V. SETS is FPA.

Related Clinical Trials

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.

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Other records listing C. B. Dumont Company, 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.

K821537HENKE DISPOSABLE SYRINGE

Related Devices (Code: FPA)

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.

K254123Ecomed Disposable Administration SetsEcomed Solutions, LLCK261530iiSure Infusion SetDeka Research and DevelopmentK252543AMSafe Administration Set (BA-70075, BA-70071-D, BA-70070, BA-70071-P, BA-70072, BA-70072-F, BA-70071-DF, BA-70071-DF-120, FE01, FE04)Amsino International, Inc.K251375PuraCath Firefly Needleless Connector IT (9005)Puracath Medical, Inc.K251257nSet+ Stabilization Set [6426733]; nSet+ Stabilization Set with nSyte Needle Free Connector (NFC) [6426731]; nSyte Needle Free Connector (NFC) [6426727]Np MedicalK250325BD Alaris Pump Infusion SetCarefusion (Bd)

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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