Aveir Introducer

FDA 510(k) Premarket Notification · Submission K211989 · Applicant: ABBOTT MEDICAL

Public Record 510(k) Submission Decision Date: 2021-07-27 510(k) record compiled from public FDA source records.

Submission Details & Decision

Normalized public record details for 510(k) notification K211989.

Source Dataset
FDA 510(k) Premarket Notifications
510(k) Number
K211989
Applicant / Sponsor
Device Name
Aveir Introducer
Product Code
DYB
Decision Date
2021-07-27
Decision / Status
Substantially Equivalent (SESE)
Advisory Committee
Cardiovascular (CV)
Clearance Type
Special
Third Party Flag
N
Date Received
2021-06-28

Related Establishments / Registrations

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