K872852 is an FDA 510(k) clearance for the EAGLE DIAGNOSTICS GLYCOHEMOGLOBIN UNITIZED TEST. This device is classified as a Assay, Glycosylated Hemoglobin (Class II - Special Controls, product code LCP).
Submitted by Sandare Chemical Co., Inc. (Desoto, US). The FDA issued a Cleared decision on September 29, 1987, 71 days after receiving the submission on July 20, 1987.
This device falls under the Hematology FDA review panel. Regulated under 21 CFR 864.7470.
| 510(k) Number | K872852 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | July 20, 1987 |
| Decision Date | September 29, 1987 |
| Days to Decision | 71 days |
| Submission Type | Traditional |
| Review Panel | Hematology (HE) |
| Summary | — |
| Product Code | LCP — Assay, Glycosylated Hemoglobin |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 864.7470 |