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.
Registration Number | 3013986346 |
FEI Number | 3013986346 |
Name | PRESSURE PRODUCTS MEDICAL DEVICE MANUFACTURING LLC |
Owner & Operator | Pressure Products Medical Device Manufacturing LLC |
Contact Address | 1 School Street Morton PA 19070 US |
Official Correspondent |
|
Registration Status | 1 |
Initial Importer | N |
Registration Expiration | 2020-04-25 |
Registration Address | 1 School Street Morton, PA 19070 US |
Establishment Type | Manufacture Medical Device |
Device Company | Device | Date |
---|---|---|
Pressure Products Medical Device Manufacturing LLC. | SafeSept® Transseptal Guidewire (SS-140) | 2022-09-14 |
Pressure Products Medical Device Manufacturing LLC | SafeSept Blunt Needle | 2021-03-05 |
PRESSURE PRODUCTS MEDICAL DEVICE MANUFACTURING LLC | TSI Transseptal Introducer | 2018-10-27 |
Pressure Products Medical Device Manufacturing LLC | TSI Transseptal Introducer | 2018-10-26 |
Pressure Products Medical Device Manufacturing LLC | TSN Transseptal Needle | 2018-02-21 |
PRESSURE PRODUCTS MEDICAL DEVICE MANUFACTURING LLC | TSN Transseptal Needle | 2018-02-21 |
Pressure Products Medical Device Manufacturing LLC | Needle Free Transseptal Cannula | 2018-02-16 |
PRESSURE PRODUCTS MEDICAL DEVICE MANUFACTURING LLC | Needle Free Transseptal Cannula | 2018-02-16 |
PRESSURE PRODUCTS MEDICAL DEVICE MANUFACTURING LLC | SafeSept Needle Free Transseptal Guidewire | 2017-12-28 |
Pressure Products Medical Device Manufacturing LLC | SafeSept Needle Free Transseptal Guidewire | 2017-12-21 |
PRESSURE PRODUCTS MEDICAL DEVICE MANUFACTURING LLC | SafeSept Transseptal Guidewire | 2017-10-23 |
Pressure Products Medical Device Manufacturing LLC | SafeSept Transseptal Guidewire | 2017-10-20 |