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FDA 510(k)

GREINER MINICOLLECT COAGULATION BLOOD COLLECTION TUBE

K-Number: K992244 · 1999-07-26

ApplicantGreiner Meditech, Inc.
Decision Date1999-07-26
Product CodeJKA
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

GREINER MINICOLLECT COAGULATION BLOOD COLLECTION TUBE is the device name listed in this FDA 510(k) record. The listed applicant is Greiner Meditech, Inc.. It received FDA 510(k) clearance on 1999-07-26 under 510(k) number K992244. The device is classified under product code JKA. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GREINER MINICOLLECT COAGULATION BLOOD COLLECTION TUBE?

GREINER MINICOLLECT COAGULATION BLOOD COLLECTION TUBE is a medical device that received FDA 510(k) clearance on 1999-07-26. The listed applicant is Greiner Meditech, Inc.. The 510(k) number is K992244.

When did GREINER MINICOLLECT COAGULATION BLOOD COLLECTION TUBE receive FDA 510(k) clearance?

GREINER MINICOLLECT COAGULATION BLOOD COLLECTION TUBE received FDA 510(k) clearance on 1999-07-26, under 510(k) number K992244.

Who is the listed applicant for GREINER MINICOLLECT COAGULATION BLOOD COLLECTION TUBE?

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

What is the FDA product code for GREINER MINICOLLECT COAGULATION BLOOD COLLECTION TUBE?

The FDA product code for GREINER MINICOLLECT COAGULATION BLOOD COLLECTION TUBE is JKA.

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Other records listing Greiner Meditech, 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.

K992145ECOMED SCALP VEIN SETK991843GREINER MINICOLLECT LITHIUM HEPARIN GEL BLOOD COLLECTION TUBEK983952GREINER VACUETTE BLOOD COLLECTION TUBEK982998GREINER MINICOLLECT SERUM GEL BLOOD COLLECTION TUBEK982999GREINER MINICOLLECT EDTA BLOOD COLLECTION TUBEK981619VACUETTE MULTIPLE SAMPLE LUER ADAPTER

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Related Devices (Code: JKA)

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.

K262215Profoject™ Safety Sliding Blood Collection SetCMT Health PTE., Ltd.K252899Female Culture Device; Male Culture Device; Transfer Device; Access DeviceZhejiang Kindly Medical Device Co., Ltd.K260128BD Preset™ and BD A-Line™ Arterial Blood Collection SyringesBecton, Dickinson and CompanyK252506BD Vacutainer® Safety-Lok™ Blood Collection Set; BD Vacutainer® Safety-Lok™ Blood Collection Set with Pre-Attached HolderBecton, Dickinson and CompanyK252378BD® MiniDraw™ Capillary Blood Collection System with BD® MiniDraw™ SST™ Capillary Blood Collection TubeBecton, Dickinson and CompanyK252040BD Vacutainer® Plasma Separator Tubes (PST™), BD Vacutainer® Sodium Heparin Blood Collection TubesBecton, Dickinson and Company

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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