Stockert Instrumente GmbH
Stockert Instrumente GmbH holds FDA 510(k) medical device clearances, first cleared 2001, most recent 2004.
Top product codes for Stockert Instrumente GmbH
Recent clearances by Stockert Instrumente GmbH
- K042374 — STOCKERT SCP RHYTHM
- K041558 — STOCKERTIR PURGE CONTROL (APC) SYSTEM
- K032213 — STOCKERT CENTRIFUGAL PUMP SYSTEM WITH TUBING CLAMP
- K023622 — STOCKERT PEDIATRIC AORTIC CANNULAE, MODEL NUMBERS A272-15 THROUGH A272-35
- K022280 — STOCKERT CORONARY PERFUSION CANNULAE
- K022321 — STOCKERT V172-28 VENOUS FEMORAL CANNULA
- K020571 — STOCKERT CENTRIFUGAL PUMP CONSOLE
- K011838 — CENTRIFUGAL PUMP
- K011088 — SIII ALARM AMPLIFIER
Data sourced from openFDA. This site is unofficial and independent of the FDA.