VARIANT(TM) HEMOGLOBIN A 1C PROGRAM
FDA 510(k) clearance K926469 · decided 1993-03-29
Clearance details
- K-number
- K926469
- Device name
- VARIANT(TM) HEMOGLOBIN A 1C PROGRAM
- Applicant
- Bio-Rad
- Decision
- Substantially Equivalent
- Date received
- 1992-12-28
- Decision date
- 1993-03-29
- Days to decision
- 91 days
- Clearance type
- Traditional
- Product code
- LCP
- Device class
- 2
- Regulation number
- 864.7470
- Medical specialty
- Hematology
- Advisory committee
- Hematology
- Location
- Hercules, CA, US
- Third-party review
- No
- Expedited review
- No
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Similar devices under this product code
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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 |