K770655 is an FDA 510(k) clearance for the LATELET DETERMIBATION KIT, UL 800. This device is classified as a Control, Platelet (Class II - Special Controls, product code GJP).
Submitted by Bd Becton Dickinson Vacutainer Systems Preanalytic (Washington, US). The FDA issued a Cleared decision on June 24, 1977, 79 days after receiving the submission on April 6, 1977.
This device falls under the Hematology FDA review panel. Regulated under 21 CFR 864.8625.
| 510(k) Number | K770655 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | April 06, 1977 |
| Decision Date | June 24, 1977 |
| Days to Decision | 79 days |
| Submission Type | Traditional |
| Review Panel | Hematology (HE) |
| Summary | — |
| Product Code | GJP — Control, Platelet |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 864.8625 |