Stoeckert Instrumente - FDA 510(k) Cleared Devices
13
Total
13
Cleared
0
Denied
FDA 510(k) Regulatory Record - Stoeckert Instrumente Cardiovascular ✕
13 devices
Cleared
Jan 29, 2001
STOCKERT A272 SERIES PEDIATRIC AORTIC CANNULAE
Cardiovascular
187d
Cleared
Jan 25, 2001
STOCKERT A242 AND A252 SERIES ARTERIAL FEMORAL CANNULAE
Cardiovascular
212d
Cleared
Aug 09, 2000
STOCKERT COMPACT SYSTEM VERSION 2.0
Cardiovascular
27d
Cleared
Dec 20, 1999
INTERFACE MODULE IDDD
Cardiovascular
136d
Cleared
Nov 23, 1999
STOCKERT POWER SUPPLY UNIT FOR S3 COMPONENTS
Cardiovascular
278d
Cleared
Sep 04, 1998
STOCKERT COMPACT SYSTEM
Cardiovascular
88d
Cleared
Feb 27, 1998
S3 MAST PUMP
Cardiovascular
249d
Cleared
Sep 10, 1997
S3 CYCLIC RPM CONTROL
Cardiovascular
138d
Cleared
Jan 10, 1997
S3 CARDIOPLEGIA CONTROL
Cardiovascular
207d
Cleared
Feb 22, 1996
STOCKERT S3 UPS, LVL CTRL BUBB. DET., DUAL PRESS. CTRL., TEMP MONT., TIMER
Cardiovascular
101d
Cleared
Feb 21, 1996
STOCKERT S3 DOUBLE HEAD PUMP MODULE
Cardiovascular
110d
Cleared
Jan 19, 1996
STOCKERT S3 ROLLER PUMP MODULE STOCKERT S3 CONSOLE
Cardiovascular
322d
Cleared
Mar 18, 1982
STOCKERT CARDIAC PACING ELECTRODES
Cardiovascular
240d