FDA 510(k)

KIT, RADIOASSAY, SERUM IRON

K-Number: K760045 · 1976-07-20

ApplicantBd Becton Dickinson Vacutainer Systems Preanalytic

Decision Date1976-07-20

Product CodeJJA

Advisory CommitteeCH

DecisionSubstantially Equivalent

Device Summary

KIT, RADIOASSAY, SERUM IRON 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 1976-07-20 under 510(k) number K760045. The device is classified under product code JJA. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KIT, RADIOASSAY, SERUM IRON?

KIT, RADIOASSAY, SERUM IRON is a medical device that received FDA 510(k) clearance on 1976-07-20. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. The 510(k) number is K760045.

When did KIT, RADIOASSAY, SERUM IRON receive FDA 510(k) clearance?

KIT, RADIOASSAY, SERUM IRON received FDA 510(k) clearance on 1976-07-20, under 510(k) number K760045.

Who is the listed applicant for KIT, RADIOASSAY, SERUM IRON?

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 KIT, RADIOASSAY, SERUM IRON?

The FDA product code for KIT, RADIOASSAY, SERUM IRON is JJA.

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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.