FUJIFILM EC-B SERIES CASETTE— 510(k) K932565
Substantially EquivalentFujifilm Medical System U.S.A., Inc.
FDA 510(k) clearance K932565 for FUJIFILM EC-B SERIES CASETTE, Substantially Equivalent on 1993-07-26. Applicant: Fujifilm Medical System U.S.A., Inc.. Device class: 2.
Clearance details
- Applicant
- Fujifilm Medical System U.S.A., Inc.
- Product code
- Code IXA
- Device class
- Class 2
- Regulation
- 21 CFR 892.1850
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Stamford, CT, US
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