FDA 510(k)

BECTON DICKINSON BLUNT STEEL CANNULA

K-Number: K944931 · 1995-08-29

ApplicantBd Becton Dickinson Vacutainer Systems Preanalytic

Decision Date1995-08-29

Product CodeFMI

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

BECTON DICKINSON BLUNT STEEL CANNULA 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 1995-08-29 under 510(k) number K944931. 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 BECTON DICKINSON BLUNT STEEL CANNULA?

BECTON DICKINSON BLUNT STEEL CANNULA is a medical device that received FDA 510(k) clearance on 1995-08-29. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. The 510(k) number is K944931.

When did BECTON DICKINSON BLUNT STEEL CANNULA receive FDA 510(k) clearance?

BECTON DICKINSON BLUNT STEEL CANNULA received FDA 510(k) clearance on 1995-08-29, under 510(k) number K944931.

Who is the listed applicant for BECTON DICKINSON BLUNT STEEL CANNULA?

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 BECTON DICKINSON BLUNT STEEL CANNULA?

The FDA product code for BECTON DICKINSON BLUNT STEEL CANNULA 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.