Stoeckert Instrumente
Stoeckert Instrumente appears in FDA public data with 0 recalls, 13 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on January 29, 2001.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 13
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K002273 | STOCKERT A272 SERIES PEDIATRIC AORTIC CANNULAE | January 29, 2001 |
| K001961 | STOCKERT A242 AND A252 SERIES ARTERIAL FEMORAL CANNULAE | January 25, 2001 |
| K002118 | STOCKERT COMPACT SYSTEM VERSION 2.0 | August 9, 2000 |
| K992635 | INTERFACE MODULE IDDD | December 20, 1999 |
| K990512 | STOCKERT POWER SUPPLY UNIT FOR S3 COMPONENTS | November 23, 1999 |
| K982014 | STOCKERT COMPACT SYSTEM | September 4, 1998 |
| K972321 | S3 MAST PUMP | February 27, 1998 |
| K971520 | S3 CYCLIC RPM CONTROL | September 10, 1997 |
| K962320 | S3 CARDIOPLEGIA CONTROL | January 10, 1997 |
| K955152 | STOCKERT S3 UPS, LVL CTRL BUBB. DET., DUAL PRESS. CTRL., TEMP MONT., TIMER | February 22, 1996 |
| K955038 | STOCKERT S3 DOUBLE HEAD PUMP MODULE | February 21, 1996 |
| K950990 | STOCKERT S3 ROLLER PUMP MODULE STOCKERT S3 CONSOLE | January 19, 1996 |
| K812049 | STOCKERT CARDIAC PACING ELECTRODES | March 18, 1982 |