K081890 is an FDA 510(k) clearance for the SYSMEX XT-SERIES IG PARAMETER,SYSMEX XT-SERIES RET-HE PARAMETER. This device is classified as a Counter, Differential Cell (Class II - Special Controls, product code GKZ).
Submitted by Sysmex America, Inc. (Mundelein, US). The FDA issued a Cleared decision on October 10, 2008, 100 days after receiving the submission on July 2, 2008.
This device falls under the Hematology FDA review panel. Regulated under 21 CFR 864.5220.
| 510(k) Number | K081890 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | July 02, 2008 |
| Decision Date | October 10, 2008 |
| Days to Decision | 100 days |
| Submission Type | Traditional |
| Review Panel | Hematology (HE) |
| Summary | Summary PDF |
| Product Code | GKZ — Counter, Differential Cell |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 864.5220 |