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FDA 510(k)

DUPONT APC BLOOD COLLECTION CONTAINER WITH THROMBOPLASTIN

K-Number: K942241 · 1994-08-18

ApplicantDupont Medical Products
Decision Date1994-08-18
Product CodeJKA
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

DUPONT APC BLOOD COLLECTION CONTAINER WITH THROMBOPLASTIN is the device name listed in this FDA 510(k) record. The listed applicant is Dupont Medical Products. It received FDA 510(k) clearance on 1994-08-18 under 510(k) number K942241. 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 DUPONT APC BLOOD COLLECTION CONTAINER WITH THROMBOPLASTIN?

DUPONT APC BLOOD COLLECTION CONTAINER WITH THROMBOPLASTIN is a medical device that received FDA 510(k) clearance on 1994-08-18. The listed applicant is Dupont Medical Products. The 510(k) number is K942241.

When did DUPONT APC BLOOD COLLECTION CONTAINER WITH THROMBOPLASTIN receive FDA 510(k) clearance?

DUPONT APC BLOOD COLLECTION CONTAINER WITH THROMBOPLASTIN received FDA 510(k) clearance on 1994-08-18, under 510(k) number K942241.

Who is the listed applicant for DUPONT APC BLOOD COLLECTION CONTAINER WITH THROMBOPLASTIN?

The FDA 510(k) record lists Dupont Medical Products as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DUPONT APC BLOOD COLLECTION CONTAINER WITH THROMBOPLASTIN?

The FDA product code for DUPONT APC BLOOD COLLECTION CONTAINER WITH THROMBOPLASTIN is JKA.

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Other records listing Dupont Medical Products 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.

K952815DUPONT LIPASE CALIBRATORK950920DUPONT DIMENSION TOTAL PROTEIN METHODK952816LIPASE FLEX REAGENT CARTRIDGEK952412DUPONT ACA(R) URINE DRUGE OS ABUSE CONTROLK945280DUPONT DIMENSION C-REACTIVE PROTEIN METHODK944932PHENOBARBITAL FLEX REAGENT CARTRIDGE

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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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