MXD100/MX 20, OR MX 30, OR MX 40 OR MX 50--(MXD 100 SERIES)— 510(k) K011111
Substantially EquivalentModular X-Ray Devices
FDA 510(k) clearance K011111 for MXD100/MX 20, OR MX 30, OR MX 40 OR MX 50--(MXD 100 SERIES), Substantially Equivalent on 2001-05-30. Applicant: Modular X-Ray Devices.
Clearance details
- Applicant
- Modular X-Ray Devices
- Product code
- Code KPR
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Roodepoort, ZA
Adverse events under product code KPR
product code KPR- Other
- 6
- Total
- 6
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.