Medical Device Manufacturer · US , Mchenry , IL

Stoeckert Instrumente - FDA 510(k) Cleared Devices

13 submissions · 13 cleared · Since 1982

Total

Cleared

Denied

Stoeckert Instrumente has 13 FDA 510(k) cleared cardiovascular devices. Based in Mchenry, US.

Historical record: 13 cleared submissions from 1982 to 2001.

Browse the complete list of FDA 510(k) cleared cardiovascular devices from this manufacturer. Filter by specialty or product code using the sidebar.

Stoeckert Instrumente is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Stoeckert Instrumente

13 devices

1-12 of 13

Cleared Jan 29, 2001

STOCKERT A272 SERIES PEDIATRIC AORTIC CANNULAE

K002273 · DWF

Cardiovascular · 187d

Cleared Jan 25, 2001

STOCKERT A242 AND A252 SERIES ARTERIAL FEMORAL CANNULAE

K001961 · DWF

Cardiovascular · 212d

Cleared Aug 09, 2000

STOCKERT COMPACT SYSTEM VERSION 2.0

K002118 · DTQ

Cardiovascular · 27d

Cleared Dec 20, 1999

INTERFACE MODULE IDDD

K992635 · KRI

Cardiovascular · 136d

Cleared Nov 23, 1999

STOCKERT POWER SUPPLY UNIT FOR S3 COMPONENTS

K990512 · KRI

Cardiovascular · 278d

Cleared Sep 04, 1998

STOCKERT COMPACT SYSTEM

Cardiovascular · 249d

Cleared Sep 10, 1997

S3 CYCLIC RPM CONTROL

K971520 · DWB

Cardiovascular · 138d

Cleared Jan 10, 1997

S3 CARDIOPLEGIA CONTROL

K962320 · DTR

Cardiovascular · 207d

Cleared Feb 22, 1996

STOCKERT S3 UPS, LVL CTRL BUBB. DET., DUAL PRESS. CTRL., TEMP MONT., TIMER

K955152 · DTW

Cardiovascular · 101d

Cleared Feb 21, 1996

STOCKERT S3 DOUBLE HEAD PUMP MODULE

K955038 · DWB

Cardiovascular · 110d

Cleared Jan 19, 1996

STOCKERT S3 ROLLER PUMP MODULE STOCKERT S3 CONSOLE

K950990 · DTQ

Cardiovascular · 322d

Stoeckert Instrumente - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Stoeckert Instrumente

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