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FDA 510(k)

VACUETTE (MULTI-USE HOLDER)

K-Number: K974873 · 1998-02-05

ApplicantGreiner Meditech, Inc.
Decision Date1998-02-05
Product CodeJKA
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

VACUETTE (MULTI-USE HOLDER) 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 1998-02-05 under 510(k) number K974873. 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 VACUETTE (MULTI-USE HOLDER)?

VACUETTE (MULTI-USE HOLDER) is a medical device that received FDA 510(k) clearance on 1998-02-05. The listed applicant is Greiner Meditech, Inc.. The 510(k) number is K974873.

When did VACUETTE (MULTI-USE HOLDER) receive FDA 510(k) clearance?

VACUETTE (MULTI-USE HOLDER) received FDA 510(k) clearance on 1998-02-05, under 510(k) number K974873.

Who is the listed applicant for VACUETTE (MULTI-USE HOLDER)?

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 VACUETTE (MULTI-USE HOLDER)?

The FDA product code for VACUETTE (MULTI-USE HOLDER) 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 SETK992244GREINER MINICOLLECT COAGULATION BLOOD COLLECTION TUBEK991843GREINER MINICOLLECT LITHIUM HEPARIN GEL BLOOD COLLECTION TUBEK983952GREINER VACUETTE BLOOD COLLECTION TUBEK982998GREINER MINICOLLECT SERUM GEL BLOOD COLLECTION TUBEK982999GREINER MINICOLLECT EDTA BLOOD COLLECTION TUBE

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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 CompanyK252378BD® MiniDraw™ Capillary Blood Collection System with BD® MiniDraw™ SST™ Capillary Blood Collection TubeBecton, Dickinson and CompanyK252506BD Vacutainer® Safety-Lok™ Blood Collection Set; BD Vacutainer® Safety-Lok™ Blood Collection Set with Pre-Attached HolderBecton, 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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