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FDA 510(k)

COMBO-FER IRON DIAGNOSTIC

K-Number: K811954 · 1981-07-27

ApplicantImmuno Assay Corp.
Decision Date1981-07-27
Product CodeJQG
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

COMBO-FER IRON DIAGNOSTIC is the device name listed in this FDA 510(k) record. The listed applicant is Immuno Assay Corp.. It received FDA 510(k) clearance on 1981-07-27 under 510(k) number K811954. The device is classified under product code JQG. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COMBO-FER IRON DIAGNOSTIC?

COMBO-FER IRON DIAGNOSTIC is a medical device that received FDA 510(k) clearance on 1981-07-27. The listed applicant is Immuno Assay Corp.. The 510(k) number is K811954.

When did COMBO-FER IRON DIAGNOSTIC receive FDA 510(k) clearance?

COMBO-FER IRON DIAGNOSTIC received FDA 510(k) clearance on 1981-07-27, under 510(k) number K811954.

Who is the listed applicant for COMBO-FER IRON DIAGNOSTIC?

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

What is the FDA product code for COMBO-FER IRON DIAGNOSTIC?

The FDA product code for COMBO-FER IRON DIAGNOSTIC is JQG.

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Other records listing Immuno Assay 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.

K833842RIA COAT DIGOXINK833745RIACOAT T-4K820089TSH (RIA) KITK820074CORTISOL (RIA) KITK811725TBG DIAGNOSTIC KITK811213T3 (RIA) KIT

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Related Devices (Code: JQG)

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.

K800710FERRITIRON KIT CAT. #RP-1100Ria Products, Inc.K800868FERRO-QUANT TM FE 59 TEST KITMallinckrodt Critical CareK790133SPINSEP-FE59Nuclear Diagnostics, Inc.K780412TOTAL IRON BINDING CAPACITYDiagnostic Corp. of America

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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