BD Kiestra IdentifA
K-Number: K222563 · 2023-08-31
ApplicantBecton, Dickinson and Company
Decision Date2023-08-31
Product CodeQQV
Advisory CommitteeMI
DecisionSubstantially Equivalent
Device Summary
BD Kiestra IdentifA is a medical device manufactured by Becton, Dickinson and Company. It received FDA 510(k) clearance on 2023-08-31 under approval number K222563. The device is classified under product code QQV. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the BD Kiestra IdentifA?
BD Kiestra IdentifA is a medical device that received FDA 510(k) clearance on 2023-08-31. It is manufactured by Becton, Dickinson and Company. The 510(k) number is K222563.
When was BD Kiestra IdentifA approved by the FDA?
BD Kiestra IdentifA received FDA 510(k) clearance on 2023-08-31, under approval number K222563.
What company makes BD Kiestra IdentifA?
BD Kiestra IdentifA is manufactured by Becton, Dickinson and Company.
What is the FDA product code for BD Kiestra IdentifA?
The FDA product code for BD Kiestra IdentifA is QQV.
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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.