GUIDANT SYNCRUS INTERNAL CARDIOVERSION SYSTEM— 510(k) K024071
Substantially EquivalentGuidant Corporation, Cardiac Surgery
FDA 510(k) clearance K024071 for GUIDANT SYNCRUS INTERNAL CARDIOVERSION SYSTEM, Substantially Equivalent on 2003-02-14. Applicant: Guidant Corporation, Cardiac Surgery.
Clearance details
- Applicant
- Guidant Corporation, Cardiac Surgery
- Product code
- Code NHW
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Location
- Santa Clara, CA, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.