Medical Device Manufacturer · SE , Bulach

Schneider (Europe) GmbH - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 1995

5

Total

5

Cleared

0

Denied

FDA 510(k) Regulatory Record - Schneider (Europe) GmbH Cardiovascular ✕

4 devices

1-4 of 4

Cleared Oct 21, 1998

DOCKING-EXTENSION WIRE

Cardiovascular · 89d

Cleared Jun 10, 1997

CLYDE CORONARY GUIDEWIRE

Cardiovascular · 119d

Cleared May 09, 1997

HANNIBAL GUIDEWIRE

Cardiovascular · 88d

Cleared Jun 08, 1995

C-THRU CORONARY GUIDE WIRE

Cardiovascular · 90d