Jostra AG is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Jostra AG - FDA 510(k) Cleared Devices
13
Total
13
Cleared
0
Denied
Jostra AG has 13 FDA 510(k) cleared cardiovascular devices. Based in Newark, US.
Historical record: 13 cleared submissions from 2000 to 2004.
Browse the complete list of FDA 510(k) cleared cardiovascular devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Jostra AG
13 devices
Cleared
Jan 30, 2004
JOSTRA SUCKERS, MODEL JS
Cardiovascular
674d
Cleared
Feb 26, 2003
QUANDROX SAFELINE HOLLOW FIBER MEMBRANE OXYGENATOR, MODEL HMO 2030
Cardiovascular
30d
Cleared
Jan 09, 2003
JOSTRA SINGLE STAGE VENOUS RETURN CATHETERS
Cardiovascular
304d
Cleared
Dec 17, 2002
JOSTRA MECC SYSTEM
Cardiovascular
88d
Cleared
Sep 11, 2002
JOSTRA VENT CATHETERS, MODELS LV & HKV
Cardiovascular
83d
Cleared
Apr 24, 2002
JOSTRA ANTEGRADE CARDIOPLEGIA CANNULA
Cardiovascular
68d
Cleared
Mar 26, 2002
JOSTRA RETROGRADE CARDIOPLEGIA CANNULAE
Cardiovascular
85d
Cleared
Feb 11, 2002
JOSTRA DUAL STAGE VENOUS RETURN CANNULAE
Cardiovascular
74d
Cleared
Dec 14, 2001
JOSTRA FLOWPROBE FP-32E
Cardiovascular
15d
Cleared
Nov 16, 2001
JOSTRA ARTERIAL PERFUSION CANNULAE
Cardiovascular
88d
Cleared
Nov 06, 2001
JOSTRA ARTERIAL PERFUSION CANNULAE, MODEL A...
Cardiovascular
85d
Cleared
Jul 11, 2001
VENOUS HARDSHELL CARDIOTOMY RESEVOIR, MODEL VHK 4201
Cardiovascular
236d
Cleared
Oct 05, 2000
ELS CANNULA (KIT), MODEL M1210-88,M1510-88
Cardiovascular
22d