Guidant Corporation, Cardiac Surgery
Guidant Corporation, Cardiac Surgery appears in FDA public data with 0 recalls, 8 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on February 8, 2008.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 8
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K080169 | HEARTSTRING III PROXIMAL SEAL SYSTEM | February 8, 2008 |
| K041340 | GUIDANT MICROWAVE ABLATION SYSTEM | July 28, 2004 |
| K023630 | ESSEX ASPIRATION/IRRIGATION INSTRUMENT WITH POSITIONING GUIDE, MODEL SY-1400 | February 20, 2003 |
| K024071 | GUIDANT SYNCRUS INTERNAL CARDIOVERSION SYSTEM | February 14, 2003 |
| K023629 | ESSEX DISSECTION CANNULA, MODEL SXD-1100, ESSEX DISSECTION TIP, MODEL SXD-1200 | November 12, 2002 |
| K022718 | VASOVIEW 6 HARVESTING CANNULA, MODELS VH-2000, VH-2001 & VH-2002 | August 28, 2002 |
| K020701 | SYNCRUS INTERNAL CARDIOVERSION SYSTEM | May 24, 2002 |
| K020143 | VASOVIEW 5 HARVESTING CANNULA | February 20, 2002 |