Submission Details
| 510(k) Number | K073309 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | November 23, 2007 |
| Decision Date | October 17, 2008 |
| Days to Decision | 329 days |
| Submission Type | Traditional |
| Review Panel | Chemistry (CH) |
| Summary | Summary PDF |
K073309 is an FDA 510(k) clearance for the ABX PENTRA HBA1C WB, CALIBRATOR, CONTROL AND HEMOLYSIS REAGENT, a Assay, Glycosylated Hemoglobin (Class II — Special Controls, product code LCP), submitted by Horiba Abx (Montpellier Cedex 4, FR). The FDA issued a Cleared decision on October 17, 2008, 329 days after receiving the submission on November 23, 2007. This device falls under the Chemistry review panel. Regulated under 21 CFR 864.7470.
| 510(k) Number | K073309 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | November 23, 2007 |
| Decision Date | October 17, 2008 |
| Days to Decision | 329 days |
| Submission Type | Traditional |
| Review Panel | Chemistry (CH) |
| Summary | Summary PDF |
| Product Code | LCP — Assay, Glycosylated Hemoglobin |
| Device Class | Class II — Special Controls |
| CFR Regulation | 21 CFR 864.7470 |