This page includes the latest FDA filings for Techdevice Corp. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.
Device Company | Device | Date |
---|---|---|
TECHDEVICE CORPORATION | Mermaid Medical® Guidewire G60235260 | 2018-07-06 |
TECHDEVICE CORPORATION | Mermaid Medical® Guidewire G60135260 | 2018-07-06 |
TECHDEVICE CORPORATION | Mermaid Medical® Guidewire G60235180 | 2018-07-06 |
TECHDEVICE CORPORATION | Mermaid Medical® Guidewire G60135180 | 2018-07-06 |
TECHDEVICE CORPORATION | Mermaid Medical® Guidewire G60235150 | 2018-07-06 |
TECHDEVICE CORPORATION | Mermaid Medical® Guidewire G60135150 | 2018-07-06 |
TECHDEVICE CORPORATION | Mermaid Medical® Guidewire G60335090 | 2018-07-06 |
TECHDEVICE CORPORATION | Mermaid Medical® Guidewire G60235090 | 2018-07-06 |
TECHDEVICE CORPORATION | Mermaid Medical® Guidewire G60135090 | 2018-07-06 |
TECHDEVICE CORPORATION | ReShape Medical™ Guidewire RSM300 | 2018-06-12 |
TECHDEVICE CORPORATION | ENDOLOGIX GUIDEWIRE | 2011-02-25 |
TECHDEVICE CORPORATION | TECHDEVICE GUIDEWIRE | 2006-03-08 |
TECHDEVICE CORPORATION | TECHDEVICE OCCLUSION BALLOON CATHETER | 2006-02-24 |
TECHDEVICE CORPORATION | TECHDEVICE GUIDEWIRE | 2006-01-31 |