FUJI COMPUTED RADIOGRAPHY (FCR) CLEARVIEW CS IMAGE READER— 510(k) K042023
Substantially EquivalentFujifilm Medical System U.S.A., Inc.
FDA 510(k) clearance K042023 for FUJI COMPUTED RADIOGRAPHY (FCR) CLEARVIEW CS IMAGE READER, Substantially Equivalent on 2004-08-25. Applicant: Fujifilm Medical System U.S.A., Inc.. Device class: 2.
Clearance details
- Applicant
- Fujifilm Medical System U.S.A., Inc.
- Product code
- Code MQB
- Device class
- Class 2
- Regulation
- 21 CFR 892.1680
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Stamford, CT, US
Recent devices under product code MQB
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