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FDA 510(k)

CIBA CORNING MAGIC LITE FERRITIN

K-Number: K873573 · 1987-10-07

ApplicantCiba Corning Diagnostics Corp.
Decision Date1987-10-07
Product CodeDBF
Advisory CommitteeIM
DecisionSubstantially Equivalent

Device Summary

CIBA CORNING MAGIC LITE FERRITIN 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 1987-10-07 under 510(k) number K873573. The device is classified under product code DBF. It was reviewed by the IM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CIBA CORNING MAGIC LITE FERRITIN?

CIBA CORNING MAGIC LITE FERRITIN is a medical device that received FDA 510(k) clearance on 1987-10-07. The listed applicant is Ciba Corning Diagnostics Corp.. The 510(k) number is K873573.

When did CIBA CORNING MAGIC LITE FERRITIN receive FDA 510(k) clearance?

CIBA CORNING MAGIC LITE FERRITIN received FDA 510(k) clearance on 1987-10-07, under 510(k) number K873573.

Who is the listed applicant for CIBA CORNING MAGIC LITE FERRITIN?

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 MAGIC LITE FERRITIN?

The FDA product code for CIBA CORNING MAGIC LITE FERRITIN is DBF.

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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: DBF)

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.

K193650LIAISON FerritinDiaSorin, Inc.K191562Yumizen C1200 Ferritin, Yumizen C1200 Transferrin, Yumizen C1200 Rheumatoid FactorHORIBA ABX SASK171642Atellica IM Ferritin AssaySiemens Healthcare Diagnostics, Inc.K121232K-ASSAY (R) FERRITIN REAGENT, K-ASSAY (R) FERRITIN CALIBRATORKamiya Biomedical CompanyK110736ADVIA CHEMISTRY FERRITIN (FRT) METHODSiemens Healthcare Diagnostics, Inc.K100538TINA-QUANT FERRITIN GEN. 4Roche Diagnostics

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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