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FDA 510(k)

IV EXTENSION SET SL

K-Number: K791930 · 1979-10-26

ApplicantAbbott Laboratories
Decision Date1979-10-26
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

IV EXTENSION SET SL is the device name listed in this FDA 510(k) record. The listed applicant is Abbott Laboratories. It received FDA 510(k) clearance on 1979-10-26 under 510(k) number K791930. 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 IV EXTENSION SET SL?

IV EXTENSION SET SL is a medical device that received FDA 510(k) clearance on 1979-10-26. The listed applicant is Abbott Laboratories. The 510(k) number is K791930.

When did IV EXTENSION SET SL receive FDA 510(k) clearance?

IV EXTENSION SET SL received FDA 510(k) clearance on 1979-10-26, under 510(k) number K791930.

Who is the listed applicant for IV EXTENSION SET SL?

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

What is the FDA product code for IV EXTENSION SET SL?

The FDA product code for IV EXTENSION SET SL is FPA.

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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

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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