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FDA 510(k)

SPECTRO FEIRITIN

K-Number: K812056 · 1981-08-12

ApplicantRamco Laboratories, Inc.
Decision Date1981-08-12
Product CodeDBF
Advisory CommitteeIM
DecisionSubstantially Equivalent

Device Summary

SPECTRO FEIRITIN is the device name listed in this FDA 510(k) record. The listed applicant is Ramco Laboratories, Inc.. It received FDA 510(k) clearance on 1981-08-12 under 510(k) number K812056. 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 SPECTRO FEIRITIN?

SPECTRO FEIRITIN is a medical device that received FDA 510(k) clearance on 1981-08-12. The listed applicant is Ramco Laboratories, Inc.. The 510(k) number is K812056.

When did SPECTRO FEIRITIN receive FDA 510(k) clearance?

SPECTRO FEIRITIN received FDA 510(k) clearance on 1981-08-12, under 510(k) number K812056.

Who is the listed applicant for SPECTRO FEIRITIN?

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

What is the FDA product code for SPECTRO FEIRITIN?

The FDA product code for SPECTRO FEIRITIN is DBF.

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Other records listing Ramco Laboratories, 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.

K983107VFEK981208TFRK910481EPO-RIAK872941SPECTRO CK864701VWF IMMUNOBLOTK861159SPECTRO VWF

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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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