ClearanceBrief
Company ยท US

Stoeckert Instrumente

FDA 510(k) clearances and medical device recalls filed under this name, 1982 to 2001. Name variants (Inc, Corp, punctuation) are merged.

13510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
DTQConsole, Heart-Lung Machine, Cardiopulmonary Bypass3
DWBPump, Blood, Cardiopulmonary Bypass, Roller Type3
DWFCatheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass2
KRIAccessory Equipment, Cardiopulmonary Bypass2
DTBPermanent Pacemaker Electrode1
DTRHeat-Exchanger, Cardiopulmonary Bypass1
DTWMonitor And/Or Control, Level Sensing, Cardiopulmonary Bypass1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Jan 29, 2001K002273STOCKERT A272 SERIES PEDIATRIC AORTIC CANNULAE
Stoeckert Instrumente
DWF
Jan 25, 2001K001961STOCKERT A242 AND A252 SERIES ARTERIAL FEMORAL CANNULAE
Stoeckert Instrumente
DWF
Aug 9, 2000K002118STOCKERT COMPACT SYSTEM VERSION 2.0
Stoeckert Instrumente
DTQ
Dec 20, 1999K992635INTERFACE MODULE IDDD
Stoeckert Instrumente
KRI
Nov 23, 1999K990512STOCKERT POWER SUPPLY UNIT FOR S3 COMPONENTS
Stoeckert Instrumente
KRI
Sep 4, 1998K982014STOCKERT COMPACT SYSTEM
Stoeckert Instrumente
DTQ
Feb 27, 1998K972321S3 MAST PUMP
Stoeckert Instrumente
DWB
Sep 10, 1997K971520S3 CYCLIC RPM CONTROL
Stoeckert Instrumente
DWB
Jan 10, 1997K962320S3 CARDIOPLEGIA CONTROL
Stoeckert Instrumente
DTR
Feb 22, 1996K955152STOCKERT S3 UPS, LVL CTRL BUBB. DET., DUAL PRESS. CTRL., TEMP MONT., TIMER
Stoeckert Instrumente
DTW
Feb 21, 1996K955038STOCKERT S3 DOUBLE HEAD PUMP MODULE
Stoeckert Instrumente
DWB
Jan 19, 1996K950990STOCKERT S3 ROLLER PUMP MODULE STOCKERT S3 CONSOLE
Stoeckert Instrumente
DTQ
Mar 18, 1982K812049STOCKERT CARDIAC PACING ELECTRODES
Stoeckert Instrumente
DTB

Latest recalls

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