THREE PHASE DIAGNOSTIC X-RAY GENERATOR MICRO-X 100— 510(k) K880524
Substantially EquivalentFischer Imaging Corp.
FDA 510(k) clearance K880524 for THREE PHASE DIAGNOSTIC X-RAY GENERATOR MICRO-X 100, Substantially Equivalent on 1988-05-04. Applicant: Fischer Imaging Corp.. Device class: 1.
Clearance details
- Applicant
- Fischer Imaging Corp.
- Product code
- Code IZO
- Device class
- Class 1
- Regulation
- 21 CFR 892.1700
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Denver, CO, US
Recent devices under product code IZO
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