K853722 is an FDA 510(k) clearance for the PLT-4 PLATELET ANALYZER. This device is classified as a Counter, Cell, Automated (particle Counter) (Class II - Special Controls, product code GKL).
Submitted by Texas Intl. Laboratories, Inc. (Houston, US). The FDA issued a Cleared decision on January 17, 1986, 134 days after receiving the submission on September 5, 1985.
This device falls under the Hematology FDA review panel. Regulated under 21 CFR 864.5200.
| 510(k) Number | K853722 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | September 05, 1985 |
| Decision Date | January 17, 1986 |
| Days to Decision | 134 days |
| Submission Type | Traditional |
| Review Panel | Hematology (HE) |
| Summary | — |
| Product Code | GKL — Counter, Cell, Automated (particle Counter) |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 864.5200 |