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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
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