Pressure Products Medical Device Manufacturing L L C

FDA Filings

This page includes the latest FDA filings for Pressure Products Medical Device Manufacturing L L C. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)
Registration Number3013986346
FEI Number3013986346
NamePRESSURE PRODUCTS MEDICAL DEVICE MANUFACTURING LLC
Owner & OperatorPressure Products Medical Device Manufacturing LLC
Contact Address1 School Street
Morton PA 19070 US
Official Correspondent
  • Andrew W Armour
  • 1-610-5432324-x
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address1 School Street
Morton, PA 19070 US
Establishment TypeManufacture Medical Device



FDA Filings

Device
Company
DeviceDate
Pressure Products Medical Device Manufacturing LLC.
SafeSeptĀ® Transseptal Guidewire (SS-140)2022-09-14
Pressure Products Medical Device Manufacturing LLC
SafeSept Blunt Needle2021-03-05
PRESSURE PRODUCTS MEDICAL DEVICE MANUFACTURING LLC
TSI Transseptal Introducer2018-10-27
Pressure Products Medical Device Manufacturing LLC
TSI Transseptal Introducer2018-10-26
Pressure Products Medical Device Manufacturing LLC
TSN Transseptal Needle2018-02-21
PRESSURE PRODUCTS MEDICAL DEVICE MANUFACTURING LLC
TSN Transseptal Needle2018-02-21
Pressure Products Medical Device Manufacturing LLC
Needle Free Transseptal Cannula2018-02-16
PRESSURE PRODUCTS MEDICAL DEVICE MANUFACTURING LLC
Needle Free Transseptal Cannula2018-02-16
PRESSURE PRODUCTS MEDICAL DEVICE MANUFACTURING LLC
SafeSept Needle Free Transseptal Guidewire2017-12-28
Pressure Products Medical Device Manufacturing LLC
SafeSept Needle Free Transseptal Guidewire2017-12-21
PRESSURE PRODUCTS MEDICAL DEVICE MANUFACTURING LLC
SafeSept Transseptal Guidewire2017-10-23
Pressure Products Medical Device Manufacturing LLC
SafeSept Transseptal Guidewire2017-10-20

Related Finance Registrations

Ā© 2022 FDA.report
This site is not affiliated with or endorsed by the FDA.