FUJI MEDICAL LASER IMAGERMULTI-FORMATTERS MF-300 AND MF-300L— 510(k) K950721
Substantially EquivalentFujifilm Medical System U.S.A., Inc.
FDA 510(k) clearance K950721 for FUJI MEDICAL LASER IMAGERMULTI-FORMATTERS MF-300 AND MF-300L, Substantially Equivalent on 1995-05-24. Applicant: Fujifilm Medical System U.S.A., Inc..
Clearance details
- Applicant
- Fujifilm Medical System U.S.A., Inc.
- Product code
- Code LMC
- 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.