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FDA 510(k)

ARTERIAL MICRO COLLECTION KIT

K-Number: K833312 · 1983-12-08

ApplicantCurrent Technologies, Inc.
Decision Date1983-12-08
Product CodeJKA
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

ARTERIAL MICRO COLLECTION KIT is the device name listed in this FDA 510(k) record. The listed applicant is Current Technologies, Inc.. It received FDA 510(k) clearance on 1983-12-08 under 510(k) number K833312. 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 ARTERIAL MICRO COLLECTION KIT?

ARTERIAL MICRO COLLECTION KIT is a medical device that received FDA 510(k) clearance on 1983-12-08. The listed applicant is Current Technologies, Inc.. The 510(k) number is K833312.

When did ARTERIAL MICRO COLLECTION KIT receive FDA 510(k) clearance?

ARTERIAL MICRO COLLECTION KIT received FDA 510(k) clearance on 1983-12-08, under 510(k) number K833312.

Who is the listed applicant for ARTERIAL MICRO COLLECTION KIT?

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

What is the FDA product code for ARTERIAL MICRO COLLECTION KIT?

The FDA product code for ARTERIAL MICRO COLLECTION KIT is JKA.

Related Clinical Trials

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.

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Other records listing Current Technologies, 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.

K810816PREFILLED ARTERIAL BLOOD SAMPLING SYRINGK802185ARTERIAL BLOOD SAMPLING KIT

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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