Stockert Instrumente GmbH is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Stockert Instrumente GmbH - FDA 510(k) Cleared Devices
9
Total
9
Cleared
0
Denied
Stockert Instrumente GmbH has 9 FDA 510(k) cleared medical devices. Based in North Attleboro, US.
Historical record: 9 cleared submissions from 2001 to 2004. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Stockert Instrumente GmbH Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Stockert Instrumente GmbH
9 devices
Cleared
Sep 23, 2004
STOCKERT SCP RHYTHM
Cardiovascular
22d
Cleared
Jul 02, 2004
STOCKERTIR PURGE CONTROL (APC) SYSTEM
Cardiovascular
22d
Cleared
Aug 29, 2003
STOCKERT CENTRIFUGAL PUMP SYSTEM WITH TUBING CLAMP
Cardiovascular
39d
Cleared
Nov 21, 2002
STOCKERT PEDIATRIC AORTIC CANNULAE, MODEL NUMBERS A272-15 THROUGH A272-35
Cardiovascular
23d
Cleared
Oct 11, 2002
STOCKERT CORONARY PERFUSION CANNULAE
Cardiovascular
88d
Cleared
Oct 09, 2002
STOCKERT V172-28 VENOUS FEMORAL CANNULA
Cardiovascular
84d
Cleared
Sep 23, 2002
STOCKERT CENTRIFUGAL PUMP CONSOLE
Cardiovascular
214d
Cleared
Feb 05, 2002
CENTRIFUGAL PUMP
Cardiovascular
238d
Cleared
May 02, 2001
SIII ALARM AMPLIFIER
Cardiovascular
22d