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FDA 510(k)

DIAGNON FERRITIN 125 I RIA KIT

K-Number: K830580 · 1983-05-05

ApplicantIagnon Corp.
Decision Date1983-05-05
Product CodeDBF
Advisory CommitteeIM
DecisionSubstantially Equivalent

Device Summary

DIAGNON FERRITIN 125 I RIA KIT is the device name listed in this FDA 510(k) record. The listed applicant is Iagnon Corp.. It received FDA 510(k) clearance on 1983-05-05 under 510(k) number K830580. 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 DIAGNON FERRITIN 125 I RIA KIT?

DIAGNON FERRITIN 125 I RIA KIT is a medical device that received FDA 510(k) clearance on 1983-05-05. The listed applicant is Iagnon Corp.. The 510(k) number is K830580.

When did DIAGNON FERRITIN 125 I RIA KIT receive FDA 510(k) clearance?

DIAGNON FERRITIN 125 I RIA KIT received FDA 510(k) clearance on 1983-05-05, under 510(k) number K830580.

Who is the listed applicant for DIAGNON FERRITIN 125 I RIA KIT?

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

What is the FDA product code for DIAGNON FERRITIN 125 I RIA KIT?

The FDA product code for DIAGNON FERRITIN 125 I RIA KIT is DBF.

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.

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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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