DUA-900A IMAGE-INTENSIFIED FLUOROSCOPIC X-RAY SYST— 510(k) K922364
Substantially EquivalentToshiba America Medical Systems, In.C
FDA 510(k) clearance K922364 for DUA-900A IMAGE-INTENSIFIED FLUOROSCOPIC X-RAY SYST, Substantially Equivalent on 1992-09-04. Applicant: Toshiba America Medical Systems, In.C.
Clearance details
- Applicant
- Toshiba America Medical Systems, In.C
- Product code
- Code IXR
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Tustin, CA, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.