FLOOR MOUNT TUBESTAND-PERFORMER-N 6610.102/S-9110— 510(k) K912515
Substantially EquivalentContinental X-Ray Corp.
FDA 510(k) clearance K912515 for FLOOR MOUNT TUBESTAND-PERFORMER-N 6610.102/S-9110, Substantially Equivalent on 1991-09-19. Applicant: Continental X-Ray Corp..
Clearance details
- Applicant
- Continental X-Ray Corp.
- Product code
- Code KPR
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Broadview, IL, US
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.