Jostra Medizintechnik AG

Jostra Medizintechnik AG holds 2 FDA 510(k) medical device clearances, cleared in 2000.

Top product codes for Jostra Medizintechnik AG

DTM — Cardiovascular1 device
KFM — Cardiovascular1 device

Recent clearances by Jostra Medizintechnik AG

K991864 — ROTAFLOW CENTRIFUGAL PUMP SYSTEMCode KFM·2000-08-31
K001787 — QUART ARTERIAL FILTER, MODEL HBF 140Code DTM·2000-06-30

Data sourced from openFDA. This site is unofficial and independent of the FDA.