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FDA 510(k)

TERRITIN RIA KIT

K-Number: K792588 · 1980-01-11

ApplicantBd Becton Dickinson Vacutainer Systems Preanalytic
Decision Date1980-01-11
Product CodeJMG
Advisory CommitteeIM
DecisionSubstantially Equivalent

Device Summary

TERRITIN RIA KIT 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 1980-01-11 under 510(k) number K792588. 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 TERRITIN RIA KIT?

TERRITIN RIA KIT is a medical device that received FDA 510(k) clearance on 1980-01-11. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. The 510(k) number is K792588.

When did TERRITIN RIA KIT receive FDA 510(k) clearance?

TERRITIN RIA KIT received FDA 510(k) clearance on 1980-01-11, under 510(k) number K792588.

Who is the listed applicant for TERRITIN RIA KIT?

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 TERRITIN RIA KIT?

The FDA product code for TERRITIN RIA KIT 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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