FDA 510(k)

RIA, T3 UPTAKE SOLID PHASE

K-Number: K781662 · 1978-11-08

ApplicantBd Becton Dickinson Vacutainer Systems Preanalytic

Decision Date1978-11-08

Product CodeKHQ

Advisory CommitteeCH

DecisionSubstantially Equivalent

Device Summary

RIA, T3 UPTAKE 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 1978-11-08 under 510(k) number K781662. The device is classified under product code KHQ. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RIA, T3 UPTAKE SOLID PHASE?

RIA, T3 UPTAKE SOLID PHASE is a medical device that received FDA 510(k) clearance on 1978-11-08. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. The 510(k) number is K781662.

When did RIA, T3 UPTAKE SOLID PHASE receive FDA 510(k) clearance?

RIA, T3 UPTAKE SOLID PHASE received FDA 510(k) clearance on 1978-11-08, under 510(k) number K781662.

Who is the listed applicant for RIA, T3 UPTAKE 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, T3 UPTAKE SOLID PHASE?

The FDA product code for RIA, T3 UPTAKE SOLID PHASE is KHQ.

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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.