Aveir Introducer
K-Number: K211989 · 2021-07-27
ApplicantABBOTT MEDICAL
Decision Date2021-07-27
Product CodeDYB
Advisory CommitteeCV
DecisionSubstantially Equivalent
Device Summary
Aveir Introducer is a medical device manufactured by ABBOTT MEDICAL. It received FDA 510(k) clearance on 2021-07-27 under approval number K211989. The device is classified under product code DYB. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Aveir Introducer?
Aveir Introducer is a medical device that received FDA 510(k) clearance on 2021-07-27. It is manufactured by ABBOTT MEDICAL. The 510(k) number is K211989.
When was Aveir Introducer approved by the FDA?
Aveir Introducer received FDA 510(k) clearance on 2021-07-27, under approval number K211989.
What company makes Aveir Introducer?
Aveir Introducer is manufactured by ABBOTT MEDICAL.
What is the FDA product code for Aveir Introducer?
The FDA product code for Aveir Introducer is DYB.
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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.