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..
Clearance details
- Applicant
- Fischer Imaging Corp.
- Product code
- Code EHD
- Advisory panel
- Dental
- 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.