MAMMOTEST PRODUCT, MODIFICATION— 510(k) K926575
Substantially EquivalentFischer Imaging Corp.
FDA 510(k) clearance K926575 for MAMMOTEST PRODUCT, MODIFICATION, Substantially Equivalent on 1993-03-30. Applicant: Fischer Imaging Corp.. Device class: 2.
Clearance details
- Applicant
- Fischer Imaging Corp.
- Product code
- Code EHD
- Device class
- Class 2
- Regulation
- 21 CFR 872.1800
- Advisory panel
- Dental
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Denver, CO, US
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