FDA 510(k)

VACUTAINER BRAND LUER ADAPTER

K-Number: K931367 · 1993-05-11

ApplicantBd Becton Dickinson Vacutainer Systems Preanalytic

Decision Date1993-05-11

Product CodeJKA

Advisory CommitteeCH

DecisionSubstantially Equivalent

Device Summary

VACUTAINER BRAND LUER ADAPTER 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 1993-05-11 under 510(k) number K931367. The device is classified under product code JKA. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VACUTAINER BRAND LUER ADAPTER?

VACUTAINER BRAND LUER ADAPTER is a medical device that received FDA 510(k) clearance on 1993-05-11. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. The 510(k) number is K931367.

When did VACUTAINER BRAND LUER ADAPTER receive FDA 510(k) clearance?

VACUTAINER BRAND LUER ADAPTER received FDA 510(k) clearance on 1993-05-11, under 510(k) number K931367.

Who is the listed applicant for VACUTAINER BRAND LUER ADAPTER?

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 VACUTAINER BRAND LUER ADAPTER?

The FDA product code for VACUTAINER BRAND LUER ADAPTER is JKA.

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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.