SINGLE PHASE DIAGNOSTIC X-RAY GENERATOR FX 350— 510(k) K880532
Substantially EquivalentFischer Imaging Corp.
FDA 510(k) clearance K880532 for SINGLE PHASE DIAGNOSTIC X-RAY GENERATOR FX 350, Substantially Equivalent on 1988-03-28. Applicant: Fischer Imaging Corp..
Clearance details
- Applicant
- Fischer Imaging Corp.
- Product code
- Code IZO
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Denver, CO, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.