FDA 510(k) Applications Submitted by Ken Peartree

FDA 510(k) Number	Submission Date	Device Name	Applicant
K190749	03/25/2019	087 Balloon Guide Catheter System	Q'Apel
K181000	04/16/2018	SelectFlex 072 Neurovascular Access System	Q'Apel
K191664	06/21/2019	SelectFlex 072 Neurovascular Access System	Q'Apel Medical
K211893	06/21/2021	SelectFlex Neurovascular Access System Family	Q'Apel Medical Inc
K192525	09/13/2019	087 Balloon Guide Catheter System	Q'Apel Medical LLC