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FDA 510(k)

TOTAL IRON BINDING CAPACITY

K-Number: K780412 · 1978-05-26

ApplicantDiagnostic Corp. of America
Decision Date1978-05-26
Product CodeJQG
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

TOTAL IRON BINDING CAPACITY is the device name listed in this FDA 510(k) record. The listed applicant is Diagnostic Corp. of America. It received FDA 510(k) clearance on 1978-05-26 under 510(k) number K780412. 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 TOTAL IRON BINDING CAPACITY?

TOTAL IRON BINDING CAPACITY is a medical device that received FDA 510(k) clearance on 1978-05-26. The listed applicant is Diagnostic Corp. of America. The 510(k) number is K780412.

When did TOTAL IRON BINDING CAPACITY receive FDA 510(k) clearance?

TOTAL IRON BINDING CAPACITY received FDA 510(k) clearance on 1978-05-26, under 510(k) number K780412.

Who is the listed applicant for TOTAL IRON BINDING CAPACITY?

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

What is the FDA product code for TOTAL IRON BINDING CAPACITY?

The FDA product code for TOTAL IRON BINDING CAPACITY is JQG.

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 Diagnostic Corp. of America 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.

K810477DCA DIGOX-SYN RIA TESTK781150RIA TSH IN HUMAN SERUM OR PLASMA

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.

K811954COMBO-FER IRON DIAGNOSTICImmuno Assay Corp.K800710FERRITIRON KIT CAT. #RP-1100Ria Products, Inc.K800868FERRO-QUANT TM FE 59 TEST KITMallinckrodt Critical CareK790133SPINSEP-FE59Nuclear Diagnostics, Inc.

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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