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FDA 510(k)

GREINER VACUETTE BLOOD COLLECTION TUBE E/EDTA K3

K-Number: K960860 · 1996-09-05

ApplicantGreiner America, Inc.
Decision Date1996-09-05
Product CodeJKA
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

GREINER VACUETTE BLOOD COLLECTION TUBE E/EDTA K3 is the device name listed in this FDA 510(k) record. The listed applicant is Greiner America, Inc.. It received FDA 510(k) clearance on 1996-09-05 under 510(k) number K960860. 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 VACUETTE BLOOD COLLECTION TUBE E/EDTA K3?

GREINER VACUETTE BLOOD COLLECTION TUBE E/EDTA K3 is a medical device that received FDA 510(k) clearance on 1996-09-05. The listed applicant is Greiner America, Inc.. The 510(k) number is K960860.

When did GREINER VACUETTE BLOOD COLLECTION TUBE E/EDTA K3 receive FDA 510(k) clearance?

GREINER VACUETTE BLOOD COLLECTION TUBE E/EDTA K3 received FDA 510(k) clearance on 1996-09-05, under 510(k) number K960860.

Who is the listed applicant for GREINER VACUETTE BLOOD COLLECTION TUBE E/EDTA K3?

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

What is the FDA product code for GREINER VACUETTE BLOOD COLLECTION TUBE E/EDTA K3?

The FDA product code for GREINER VACUETTE BLOOD COLLECTION TUBE E/EDTA K3 is JKA.

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Other records listing Greiner America, 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.

K971220GREINER VACUETTE BLOOD COLLECTION TUBEK971239GREINER VACUETTE BLOOD COLLECTION TUBEK971236GREINER VACUETTE BLOOD COLLECTION TUBEK971221GREINER VACUETTE BLOOD COLLECTION TUBEK960857GREINER VACUETTE BLOOD COLLECTION TUBE W/LITHIUM HEPARIN & GEL SEPARATORK960858GREINER VACUTTE BLOOD COLLECTION TUBE W/ CLOT ACTIVATOR & GEL SEPARATOR

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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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