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FDA 510(k)

CIBA CORNING BLOOD COLLECTION CAPILLARY TUBE

K-Number: K883813 · 1988-11-10

ApplicantCiba Corning Diagnostics Corp.
Decision Date1988-11-10
Product CodeJKA
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

CIBA CORNING BLOOD COLLECTION CAPILLARY TUBE is the device name listed in this FDA 510(k) record. The listed applicant is Ciba Corning Diagnostics Corp.. It received FDA 510(k) clearance on 1988-11-10 under 510(k) number K883813. 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 CIBA CORNING BLOOD COLLECTION CAPILLARY TUBE?

CIBA CORNING BLOOD COLLECTION CAPILLARY TUBE is a medical device that received FDA 510(k) clearance on 1988-11-10. The listed applicant is Ciba Corning Diagnostics Corp.. The 510(k) number is K883813.

When did CIBA CORNING BLOOD COLLECTION CAPILLARY TUBE receive FDA 510(k) clearance?

CIBA CORNING BLOOD COLLECTION CAPILLARY TUBE received FDA 510(k) clearance on 1988-11-10, under 510(k) number K883813.

Who is the listed applicant for CIBA CORNING BLOOD COLLECTION CAPILLARY TUBE?

The FDA 510(k) record lists Ciba Corning Diagnostics Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CIBA CORNING BLOOD COLLECTION CAPILLARY TUBE?

The FDA product code for CIBA CORNING BLOOD COLLECTION CAPILLARY TUBE is JKA.

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Other records listing Ciba Corning Diagnostics Corp. 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.

K962559ACS CORTISOL IMMUNOASSAYK963251CIBA CORNING ACS;180 DPD ASSAYK961807CERTAIN HCT LEVEL A & LEVEL B/CVM HCT LEVELS 1,2,3, & 4K961657CIBA CORNING 400 SYSTEMK962021CIBA CORNING 348 SYSTEMK962126ACS CKMB II IMMUNOASSAY

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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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