XIMX SYSTEM— 510(k) K002100
Substantially EquivalentMedical Manager Research Development
FDA 510(k) clearance K002100 for XIMX SYSTEM, Substantially Equivalent on 2000-08-25. Applicant: Medical Manager Research Development.
Clearance details
- Applicant
- Medical Manager Research Development
- Product code
- Code LLZ
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Washington, DC, US
Adverse events under product code LLZ
product code LLZ- Death
- 13
- Total
- 13
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.