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FDA 510(k)

CHURCHILL FEMALE LUER LOCK CAP

K-Number: K861439 · 1986-05-06

ApplicantChurchill Corp.
Decision Date1986-05-06
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

CHURCHILL FEMALE LUER LOCK CAP is the device name listed in this FDA 510(k) record. The listed applicant is Churchill Corp.. It received FDA 510(k) clearance on 1986-05-06 under 510(k) number K861439. 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 CHURCHILL FEMALE LUER LOCK CAP?

CHURCHILL FEMALE LUER LOCK CAP is a medical device that received FDA 510(k) clearance on 1986-05-06. The listed applicant is Churchill Corp.. The 510(k) number is K861439.

When did CHURCHILL FEMALE LUER LOCK CAP receive FDA 510(k) clearance?

CHURCHILL FEMALE LUER LOCK CAP received FDA 510(k) clearance on 1986-05-06, under 510(k) number K861439.

Who is the listed applicant for CHURCHILL FEMALE LUER LOCK CAP?

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

What is the FDA product code for CHURCHILL FEMALE LUER LOCK CAP?

The FDA product code for CHURCHILL FEMALE LUER LOCK CAP is FPA.

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Other records listing Churchill Corp. 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.

K880026CHURCHILL 0.22 MICRON LIQUID COMPACT FILTER SETSK880051ENTERAL BAG/SETK880025CHURCHILL 0.22 MICRON LIQUID FILTER SETSK880027CHURCHILL 1.2 MICRON LIQUID FILTER SETK870395CHURCHILL PARENTERAL NUTRITION BAG - EVAK872585CHURCHILL-CATH

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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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