VARIANT HEMOGLOBINOPATHY PROGRAM
FDA 510(k) clearance K954048 · decided 1995-11-20
Clearance details
- K-number
- K954048
- Device name
- VARIANT HEMOGLOBINOPATHY PROGRAM
- Applicant
- Bio-Rad
- Decision
- Substantially Equivalent
- Date received
- 1995-08-28
- Decision date
- 1995-11-20
- Days to decision
- 84 days
- Clearance type
- Traditional
- Product code
- GKA
- Device class
- 2
- Regulation number
- 864.7415
- Medical specialty
- Hematology
- Advisory committee
- Hematology
- Location
- Hercules, CA, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.
PMA approvals by this applicant
| Record | Firm | Date |
|---|---|---|
| BIO-RAD CYCLOSPORINE BY HPLC TEST (P880032/S002) | Bio-Rad | 1996-03-01 |
| BIO-RAD CYCLOSPORINE BY HPLC TEST (P880032/S001) | Bio-Rad | 1991-03-14 |
| BIO-RAD CYCLOSPORINE BY HPLC TEST (P880032) | Bio-Rad | 1989-07-24 |