Medical Device Manufacturer · US , Newark , DE

Jostra Medizintechnik AG - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2000

Recent clearances: ROTAFLOW CENTRIFUGAL PUMP SYSTEM, QUART ARTERIAL FILTER, MODEL HBF 140

View 2 510(k) Devices ↓

2

Total

2

Cleared

0

Denied

FDA 510(k) Regulatory Record - Jostra Medizintechnik AG Cardiovascular ✕

2 devices

1-2 of 2

Cleared Aug 31, 2000

ROTAFLOW CENTRIFUGAL PUMP SYSTEM

Cardiovascular · 457d

Cleared Jun 30, 2000

QUART ARTERIAL FILTER, MODEL HBF 140

Cardiovascular · 17d