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FDA 510(k)

PREFILLED ARTERIAL BLOOD SAMPLING SYRING

K-Number: K810816 · 1981-04-07

ApplicantCurrent Technologies, Inc.
Decision Date1981-04-07
Product CodeJKA
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

PREFILLED ARTERIAL BLOOD SAMPLING SYRING 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 1981-04-07 under 510(k) number K810816. 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 PREFILLED ARTERIAL BLOOD SAMPLING SYRING?

PREFILLED ARTERIAL BLOOD SAMPLING SYRING is a medical device that received FDA 510(k) clearance on 1981-04-07. The listed applicant is Current Technologies, Inc.. The 510(k) number is K810816.

When did PREFILLED ARTERIAL BLOOD SAMPLING SYRING receive FDA 510(k) clearance?

PREFILLED ARTERIAL BLOOD SAMPLING SYRING received FDA 510(k) clearance on 1981-04-07, under 510(k) number K810816.

Who is the listed applicant for PREFILLED ARTERIAL BLOOD SAMPLING SYRING?

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 PREFILLED ARTERIAL BLOOD SAMPLING SYRING?

The FDA product code for PREFILLED ARTERIAL BLOOD SAMPLING SYRING 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.

K833312ARTERIAL MICRO COLLECTION KITK802185ARTERIAL 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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