FDA 510(k)

MICROTAINER BRAND TUBE WITH EDTA

K-Number: K931368 · 1993-09-28

ApplicantBd Becton Dickinson Vacutainer Systems Preanalytic

Decision Date1993-09-28

Product CodeJKA

Advisory CommitteeCH

DecisionSubstantially Equivalent

Device Summary

MICROTAINER BRAND TUBE WITH EDTA 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 1993-09-28 under 510(k) number K931368. 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 MICROTAINER BRAND TUBE WITH EDTA?

MICROTAINER BRAND TUBE WITH EDTA is a medical device that received FDA 510(k) clearance on 1993-09-28. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. The 510(k) number is K931368.

When did MICROTAINER BRAND TUBE WITH EDTA receive FDA 510(k) clearance?

MICROTAINER BRAND TUBE WITH EDTA received FDA 510(k) clearance on 1993-09-28, under 510(k) number K931368.

Who is the listed applicant for MICROTAINER BRAND TUBE WITH EDTA?

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 MICROTAINER BRAND TUBE WITH EDTA?

The FDA product code for MICROTAINER BRAND TUBE WITH EDTA 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.