KYOKKO SPEC-SERIES INTENSIFY SCREENS-SPEC,SUPER SPEC
FDA 510(k) clearance K943821 · decided 1994-08-22
Clearance details
- K-number
- K943821
- Device name
- KYOKKO SPEC-SERIES INTENSIFY SCREENS-SPEC,SUPER SPEC
- Applicant
- Fujifilm Medical System U.S.A., Inc.
- Decision
- Substantially Equivalent
- Date received
- 1994-06-15
- Decision date
- 1994-08-22
- Days to decision
- 68 days
- Clearance type
- Traditional
- Product code
- EAM
- Device class
- 1
- Regulation number
- 892.1960
- Medical specialty
- Radiology
- Advisory committee
- Radiology
- Location
- Stamford, CT, US
- Third-party review
- No
- Expedited review
- No
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Similar devices under this product code
Devices cleared under the same product code - the starting set for predicate research.
Recalls involving this device
No recalls on record reference this clearance.
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 |