FDA 510(k)

BD MICROTAINER MAP MICROTUBE FOR AUTOMATED PROCESS, MODEL 363706

K-Number: K093972 · 2010-01-21

Decision Date2010-01-21

Product CodeJKA

Advisory CommitteeCH

DecisionSubstantially Equivalent

Device Summary

BD MICROTAINER MAP MICROTUBE FOR AUTOMATED PROCESS, MODEL 363706 is the device name listed in this FDA 510(k) record. The listed applicant is Becton, Dickinson & CO. It received FDA 510(k) clearance on 2010-01-21 under 510(k) number K093972. 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 BD MICROTAINER MAP MICROTUBE FOR AUTOMATED PROCESS, MODEL 363706?

BD MICROTAINER MAP MICROTUBE FOR AUTOMATED PROCESS, MODEL 363706 is a medical device that received FDA 510(k) clearance on 2010-01-21. The listed applicant is Becton, Dickinson & CO. The 510(k) number is K093972.

When did BD MICROTAINER MAP MICROTUBE FOR AUTOMATED PROCESS, MODEL 363706 receive FDA 510(k) clearance?

BD MICROTAINER MAP MICROTUBE FOR AUTOMATED PROCESS, MODEL 363706 received FDA 510(k) clearance on 2010-01-21, under 510(k) number K093972.

Who is the listed applicant for BD MICROTAINER MAP MICROTUBE FOR AUTOMATED PROCESS, MODEL 363706?

The FDA 510(k) record lists Becton, Dickinson & CO as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BD MICROTAINER MAP MICROTUBE FOR AUTOMATED PROCESS, MODEL 363706?

The FDA product code for BD MICROTAINER MAP MICROTUBE FOR AUTOMATED PROCESS, MODEL 363706 is JKA.

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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.