K000897 is an FDA 510(k) clearance for the CALIBRITE PERCP-CY5.5 BEADS AND FACSCOMP SOFTWARE. This device is classified as a Counter, Differential Cell (Class II - Special Controls, product code GKZ).
Submitted by Bd Biosciences (San Jose, US). The FDA issued a Cleared decision on May 5, 2000, 45 days after receiving the submission on March 21, 2000.
This device falls under the Hematology FDA review panel. Regulated under 21 CFR 864.5220.
| 510(k) Number | K000897 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | March 21, 2000 |
| Decision Date | May 05, 2000 |
| Days to Decision | 45 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 |