FUJI DAYLIGHT CASSETTE MULTI-LOADER— 510(k) K933408
Substantially EquivalentFujifilm Medical System U.S.A., Inc.
FDA 510(k) clearance K933408 for FUJI DAYLIGHT CASSETTE MULTI-LOADER, Substantially Equivalent on 1993-08-16. Applicant: Fujifilm Medical System U.S.A., Inc..
Clearance details
- Applicant
- Fujifilm Medical System U.S.A., Inc.
- Product code
- Code IXW
- 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.