FDA 510(k) Applications Submitted by Pressure Products Medical Device Manufacturing LLC

FDA 510(k) Number	Submission Date	Device Name	Applicant
K210328	02/04/2021	SafeSept Blunt Needle	Pressure Products Medical Device Manufacturing LLC
K170671	03/06/2017	SafeSept Transseptal Guidewire	Pressure Products Medical Device Manufacturing LLC
K181031	04/18/2018	TSI Transseptal Introducer	Pressure Products Medical Device Manufacturing LLC
K172893	09/22/2017	SafeSept Needle Free Transseptal Guidewire	Pressure Products Medical Device Manufacturing LLC
K172934	09/25/2017	Needle Free Transseptal Cannula	Pressure Products Medical Device Manufacturing LLC
K172950	09/26/2017	TSN Transseptal Needle	Pressure Products Medical Device Manufacturing LLC