Schneider Intl., Ltd. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Schneider Intl., Ltd. - FDA 510(k) Cleared Devices
22
Total
22
Cleared
0
Denied
Schneider Intl., Ltd. has 22 FDA 510(k) cleared cardiovascular devices. Based in Minneapolis, US.
Historical record: 22 cleared submissions from 1989 to 1995.
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 - Schneider Intl., Ltd.
22 devices
Cleared
Jan 11, 1995
BILIARY ENDOPROSTHESES W/UNISTEP DELIVERY SYSTEM
Gastroenterology & Urology
807d
Cleared
Jun 23, 1993
SCHNEIDER MAGNUM PERIPHERAL RECANALIZATION GUIDEWI
Cardiovascular
85d
Cleared
Jun 07, 1993
SCHNEIDER SOFTIP SST ANGIOGRAPHIC (DIAG) CATHETER
Cardiovascular
192d
Cleared
Jun 07, 1993
SCHNEIDER MATCH-35 PERCUTANEOUS TRANSLUMINAL ANGIO
Cardiovascular
171d
Cleared
Feb 12, 1993
SCHNEIDER HYDRO-SIL GUIDEWIRE
Cardiovascular
88d
Cleared
Dec 08, 1992
SCHNEIDER SOLID-7 SOPTIP GUIDING CATHETER
Cardiovascular
89d
Cleared
Jul 21, 1992
TOTAL CROSS .021 PERCUT. TRANSLUMINAL ANGIO. CATH.
Cardiovascular
95d
Cleared
Jun 17, 1992
SCHNEIDER MONORAIL 421 PERCU TRANS ANGIO (PTA) BAL
Cardiovascular
54d
Cleared
Mar 16, 1992
SCHNEIDER 8 FR. STAMINA(TM) GUIDING CATHETER
Cardiovascular
62d
Cleared
Feb 11, 1992
PTA BALLOON CATHETER
Cardiovascular
77d
Cleared
Dec 06, 1991
SCHNEIDER SOFTIP(R) A+(TM) ANGIOGRAPHIC CATHETER
Cardiovascular
88d
Cleared
Oct 10, 1991
SCHNEIDER MATCH-35(TM) PERCU TRANS ANGIOPLAS CATH
Cardiovascular
78d