This page includes the latest FDA filings for Flowcardia Inc. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.
Device Company | Device | Date |
---|---|---|
FLOWCARDIA, INC. | THE CROSSER S6 CATHETER, THE CROSSER SYSTEM ELECTRONICS, MODEL CRUS6, GEN200 | 2010-02-17 |
FLOWCARDIA, INC. | FLOWCARDIA FLOWMATER INJECTOR, MODEL INJ 100 | 2009-06-19 |
FLOWCARDIA, INC. | THE CROSSER 14 OTW CATHETER, MODEL CRU014 | 2009-05-29 |
FLOWCARDIA, INC. | MODIFICATION TO THE CROSSER SYSTEM | 2009-05-15 |
FLOWCARDIA, INC. | MICROSHEATH LP AND LP-AT | 2008-07-25 |
FLOWCARDIA, INC. | CROSSER LP SYSTEM | 2008-06-20 |
FLOWCARDIA, INC. | THE CROSSER SYSTEM | 2007-12-07 |
FLOWCARDIA INC | THE CROSSER CATHETER, MODEL CR1100 AND SYSTEM ELECTRONICS, MODEL FG1002-02 | 2007-01-19 |
FLOWCARDIA, INC. | VP SHEATH | 2005-10-31 |
FLOWCARDIA, INC. | VP WIRE GW140ST (.014 165CM, STANDAR), MODEL GW140ST; VP WIRE GW140SO (.014 165CM, SOFT) MODEL GW140SO | 2005-07-15 |
NCAGE Code | 4VM26 | FLOWCARDIA INC. |
CAGE Code | 4VM26 | FLOWCARDIA, INC. |
DUNS | 129386012 | FLOWCARDIA, INC. |