FUJI COMPUTED RADIOGRAPHY FCR/DICOM GATEWAY UNIT CR-DM666— 510(k) K970293
Substantially EquivalentFujifilm Medical System U.S.A., Inc.
FDA 510(k) clearance K970293 for FUJI COMPUTED RADIOGRAPHY FCR/DICOM GATEWAY UNIT CR-DM666, Substantially Equivalent on 1997-03-21. Applicant: Fujifilm Medical System U.S.A., Inc.. Device class: 1.
Clearance details
- Applicant
- Fujifilm Medical System U.S.A., Inc.
- Product code
- Code LMD
- Device class
- Class 1
- Regulation
- 21 CFR 892.2020
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Stamford, CT, US
Recent devices under product code LMD
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