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FDA 510(k)

BLOOD COLLECTING NEEDLE

K-Number: K855248 · 1986-02-26

ApplicantChurchill Corp.
Decision Date1986-02-26
Product CodeFMI
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

BLOOD COLLECTING NEEDLE is the device name listed in this FDA 510(k) record. The listed applicant is Churchill Corp.. It received FDA 510(k) clearance on 1986-02-26 under 510(k) number K855248. The device is classified under product code FMI. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BLOOD COLLECTING NEEDLE?

BLOOD COLLECTING NEEDLE is a medical device that received FDA 510(k) clearance on 1986-02-26. The listed applicant is Churchill Corp.. The 510(k) number is K855248.

When did BLOOD COLLECTING NEEDLE receive FDA 510(k) clearance?

BLOOD COLLECTING NEEDLE received FDA 510(k) clearance on 1986-02-26, under 510(k) number K855248.

Who is the listed applicant for BLOOD COLLECTING NEEDLE?

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 BLOOD COLLECTING NEEDLE?

The FDA product code for BLOOD COLLECTING NEEDLE is FMI.

Related Clinical Trials

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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: FMI)

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.

K261266MOWANA™ Auto DuoPENTAMASTER MEDIQ SDN BHDK261719Promisemed X-Safety Pen NeedlePromisemed Hangzhou Meditech Co., Ltd.K262427Pen Needle (Ordinary Type I, Safety Type IIA, Safety Type IIB, Safety Type IIIA, Safety Type IIIB, Safety Type IV, Safety Type V, Ordinary Type VIA, Ordinary Type VIB, Ordinary Type VIC, Safety Type VII, Ordinary Type IB, Safety type VIII, Safety Type IX, Safety Type X, Ordinary Type XI, Safety Type XII)Hh Global Technology, Inc.K260933Safety Sterile Hypodermic Needles (NR-S1816R, NR-S1916R, NR-S1925R, NR-S1938R, NR-S2016R, NR-S2025R, NR-S2038R, NR-S2051R, NR-S2116R, NR-S2125R, NR-S2138R, NR-S2151R, NR-S2216R, NR-S2225R, NR-S2238R, NR-S2251R, NR-S2316R, NR-S2325R, NR-S2338R, NR-S2351R, NR-S2516R, NR-S2525R, NR-S2538R, NR-S2551R, NR-S2516T, NR-S2525T, NR-S2538T, NR-S2551T)Hangzhou Qiantang Longyue Biotechnology Co., Ltd.K261829Profoject™ Dual-Safety Pen NeedlesCMT Health PTE., Ltd.K260739Profoject™ Pen Needles (Model A; Model B)CMT Health PTE., Ltd.

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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