Stockert Instrumente GmbH

9 FDA 510(k) medical device clearances.

Top product codes for Stockert Instrumente GmbH

Recent clearances by Stockert Instrumente GmbH

K042374 — STOCKERT SCP RHYTHM DWA · 2004-09-23
K041558 — STOCKERTIR PURGE CONTROL (APC) SYSTEM DTW · 2004-07-02
K032213 — STOCKERT CENTRIFUGAL PUMP SYSTEM WITH TUBING CLAMP DWA · 2003-08-29
K023622 — STOCKERT PEDIATRIC AORTIC CANNULAE, MODEL NUMBERS A272-15 THROUGH A272-35 DWF · 2002-11-21
K022280 — STOCKERT CORONARY PERFUSION CANNULAE DWF · 2002-10-11
K022321 — STOCKERT V172-28 VENOUS FEMORAL CANNULA DWF · 2002-10-09
K020571 — STOCKERT CENTRIFUGAL PUMP CONSOLE DTQ · 2002-09-23
K011838 — CENTRIFUGAL PUMP DWA · 2002-02-05
K011088 — SIII ALARM AMPLIFIER DTQ · 2001-05-02

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