K991402 is an FDA 510(k) clearance for the DAKO MOUSE ANTI-HUMAN T-CELL, CD3/RPE-CY5, CLONE UCHT1 & DAKO MOUSE ANTI-HUMAN T-CELL, CD3/RPE, CLONE UCHT1. This device is classified as a Counter, Differential Cell (Class II - Special Controls, product code GKZ).
Submitted by Dako Corp. (Carpinteria, US). The FDA issued a Cleared decision on June 21, 1999, 60 days after receiving the submission on April 22, 1999.
This device falls under the Hematology FDA review panel. Regulated under 21 CFR 864.5220.
| 510(k) Number | K991402 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | April 22, 1999 |
| Decision Date | June 21, 1999 |
| Days to Decision | 60 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 |