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FDA 510(k)

TURN NEEDLE INTRAVENOUS CANNUL, NUB, W/TUBING INTE

K-Number: K844917 · 1985-02-07

ApplicantTurn Needle Intl., Inc.
Decision Date1985-02-07
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

TURN NEEDLE INTRAVENOUS CANNUL, NUB, W/TUBING INTE is the device name listed in this FDA 510(k) record. The listed applicant is Turn Needle Intl., Inc.. It received FDA 510(k) clearance on 1985-02-07 under 510(k) number K844917. 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 TURN NEEDLE INTRAVENOUS CANNUL, NUB, W/TUBING INTE?

TURN NEEDLE INTRAVENOUS CANNUL, NUB, W/TUBING INTE is a medical device that received FDA 510(k) clearance on 1985-02-07. The listed applicant is Turn Needle Intl., Inc.. The 510(k) number is K844917.

When did TURN NEEDLE INTRAVENOUS CANNUL, NUB, W/TUBING INTE receive FDA 510(k) clearance?

TURN NEEDLE INTRAVENOUS CANNUL, NUB, W/TUBING INTE received FDA 510(k) clearance on 1985-02-07, under 510(k) number K844917.

Who is the listed applicant for TURN NEEDLE INTRAVENOUS CANNUL, NUB, W/TUBING INTE?

The FDA 510(k) record lists Turn Needle Intl., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TURN NEEDLE INTRAVENOUS CANNUL, NUB, W/TUBING INTE?

The FDA product code for TURN NEEDLE INTRAVENOUS CANNUL, NUB, W/TUBING INTE 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 Turn Needle Intl., 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.

K850503SECU-TAPE UNIVERSAL FLEXIBLE MEDICAL CLAMPS

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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