FUJI COMPUTED RADIOGRAPHY DUAL SIDE READING, BOTH SIDE READING, FCR 5501D DUAL SIDE READER
FDA 510(k) clearance K993861 · decided 2000-02-10
Clearance details
- K-number
- K993861
- Device name
- FUJI COMPUTED RADIOGRAPHY DUAL SIDE READING, BOTH SIDE READING, FCR 5501D DUAL SIDE READER
- Applicant
- Fujifilm Medical System U.S.A., Inc.
- Decision
- Substantially Equivalent
- Date received
- 1999-11-15
- Decision date
- 2000-02-10
- Days to decision
- 87 days
- Clearance type
- Traditional
- Product code
- MQB
- Device class
- 2
- Regulation number
- 892.1680
- Medical specialty
- Radiology
- Advisory committee
- Radiology
- Location
- Stamford, CT, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
| Record | Firm | Date |
|---|---|---|
| Genital Protector Shield used with Fuji Computed Radiography (FCR) system models 5501D and recall (Z-0055-05) | Fujifilm Medical System USA, Inc. | 2004-10-28 |
PMA approvals by this applicant
| Record | Firm | Date |
|---|---|---|
| FULL FIELD DIGITAL MAMMOGRAPHY (P050014/S002) | Fujifilm Medical System U.S.A., Inc. | 2009-08-11 |
| FUJI COMPUTED RADIOGRAPHY MAMMOGRAPHY SUITE (P050014/S001) | Fujifilm Medical System U.S.A., Inc. | 2009-01-09 |
| FUJI'S COMPUTED RADIOGRAPHY MAMMOGRAPHY SUITE (FCRMS) (P050014) | Fujifilm Medical System U.S.A., Inc. | 2006-07-10 |