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FDA 510(k)

CHURCHILL-HS SUSPENDED NON-VENTED IV SET

K-Number: K854630 · 1985-12-10

ApplicantChurchill Corp.
Decision Date1985-12-10
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

CHURCHILL-HS SUSPENDED NON-VENTED IV SET is the device name listed in this FDA 510(k) record. The listed applicant is Churchill Corp.. It received FDA 510(k) clearance on 1985-12-10 under 510(k) number K854630. 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-HS SUSPENDED NON-VENTED IV SET?

CHURCHILL-HS SUSPENDED NON-VENTED IV SET is a medical device that received FDA 510(k) clearance on 1985-12-10. The listed applicant is Churchill Corp.. The 510(k) number is K854630.

When did CHURCHILL-HS SUSPENDED NON-VENTED IV SET receive FDA 510(k) clearance?

CHURCHILL-HS SUSPENDED NON-VENTED IV SET received FDA 510(k) clearance on 1985-12-10, under 510(k) number K854630.

Who is the listed applicant for CHURCHILL-HS SUSPENDED NON-VENTED IV SET?

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-HS SUSPENDED NON-VENTED IV SET?

The FDA product code for CHURCHILL-HS SUSPENDED NON-VENTED IV SET 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 SETSK880025CHURCHILL 0.22 MICRON LIQUID FILTER SETSK880051ENTERAL BAG/SETK880027CHURCHILL 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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