PIONEER TC8080, COMPANION III— 510(k) K053648
Substantially EquivalentViasys Neuro Care
FDA 510(k) clearance K053648 for PIONEER TC8080, COMPANION III, Substantially Equivalent on 2006-01-24. Applicant: Viasys Neuro Care.
Clearance details
- Applicant
- Viasys Neuro Care
- Product code
- Code IYN
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Abbreviated
- Location
- Stoughton, WI, US
Adverse events under product code IYN
product code IYN- Death
- 25
- Injury
- 163
- Malfunction
- 1,538
- Other
- 4
- Total
- 1,730
Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →
Data sourced from openFDA. This site is unofficial and independent of the FDA.