KYOKKO BLUE SERIES INTENSIFYING SCREENS— 510(k) K942805
Substantially EquivalentFujifilm Medical System U.S.A., Inc.
FDA 510(k) clearance K942805 for KYOKKO BLUE SERIES INTENSIFYING SCREENS, Substantially Equivalent on 1994-07-29. Applicant: Fujifilm Medical System U.S.A., Inc..
Clearance details
- Applicant
- Fujifilm Medical System U.S.A., Inc.
- Product code
- Code EAM
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Stamford, CT, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.