DCX-100 CHEST UNIT-GL-5000M— 510(k) K841923
Substantially EquivalentTransworld X-Ray Corp.
FDA 510(k) clearance K841923 for DCX-100 CHEST UNIT-GL-5000M, Substantially Equivalent on 1984-08-10. Applicant: Transworld X-Ray Corp..
Clearance details
- Applicant
- Transworld X-Ray Corp.
- Product code
- Code KPR
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Walker, MI, 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.