K841852 is an FDA 510(k) clearance for the AUTOLYZER 800. This device is classified as a Counter, Differential Cell (Class II - Special Controls, product code GKZ).
Submitted by Geometric Data, Div. Smithkline Corp. (Walker, US). The FDA issued a Cleared decision on September 5, 1984, 125 days after receiving the submission on May 3, 1984.
This device falls under the Hematology FDA review panel. Regulated under 21 CFR 864.5220.
| 510(k) Number | K841852 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | May 03, 1984 |
| Decision Date | September 05, 1984 |
| Days to Decision | 125 days |
| Submission Type | Traditional |
| Review Panel | Hematology (HE) |
| Summary | — |
| Product Code | GKZ — Counter, Differential Cell |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 864.5220 |