FDA 510(k)

NEEDLE, TRUCARE VACUTAINER

K-Number: K790086 · 1979-02-08

ApplicantBd Becton Dickinson Vacutainer Systems Preanalytic

Decision Date1979-02-08

Product CodeFMI

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

NEEDLE, TRUCARE VACUTAINER 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 1979-02-08 under 510(k) number K790086. The device is classified under product code FMI. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NEEDLE, TRUCARE VACUTAINER?

NEEDLE, TRUCARE VACUTAINER is a medical device that received FDA 510(k) clearance on 1979-02-08. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. The 510(k) number is K790086.

When did NEEDLE, TRUCARE VACUTAINER receive FDA 510(k) clearance?

NEEDLE, TRUCARE VACUTAINER received FDA 510(k) clearance on 1979-02-08, under 510(k) number K790086.

Who is the listed applicant for NEEDLE, TRUCARE VACUTAINER?

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 NEEDLE, TRUCARE VACUTAINER?

The FDA product code for NEEDLE, TRUCARE VACUTAINER is FMI.

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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.