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FDA 510(k)

RIA KIT, FERRITIN SOLID PHASE

K-Number: K781946 · 1979-01-10

ApplicantBd Becton Dickinson Vacutainer Systems Preanalytic
Decision Date1979-01-10
Product CodeJMG
Advisory CommitteeIM
DecisionSubstantially Equivalent

Device Summary

RIA KIT, FERRITIN SOLID PHASE is the device name listed in this FDA 510(k) record. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. It received FDA 510(k) clearance on 1979-01-10 under 510(k) number K781946. The device is classified under product code JMG. It was reviewed by the IM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RIA KIT, FERRITIN SOLID PHASE?

RIA KIT, FERRITIN SOLID PHASE is a medical device that received FDA 510(k) clearance on 1979-01-10. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. The 510(k) number is K781946.

When did RIA KIT, FERRITIN SOLID PHASE receive FDA 510(k) clearance?

RIA KIT, FERRITIN SOLID PHASE received FDA 510(k) clearance on 1979-01-10, under 510(k) number K781946.

Who is the listed applicant for RIA KIT, FERRITIN SOLID PHASE?

The FDA 510(k) record lists Bd Becton Dickinson Vacutainer Systems Preanalytic as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for RIA KIT, FERRITIN SOLID PHASE?

The FDA product code for RIA KIT, FERRITIN SOLID PHASE is JMG.

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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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