K880270 is an FDA 510(k) clearance for the MSI-DIFF PLUS. This device is classified as a Mixture, Hematology Quality Control (Class II - Special Controls, product code JPK).
Submitted by Medical Specialties, Inc. (South Plainfield, US). The FDA issued a Cleared decision on March 1, 1988, 40 days after receiving the submission on January 21, 1988.
This device falls under the Hematology FDA review panel. Regulated under 21 CFR 864.8625.
| 510(k) Number | K880270 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | January 21, 1988 |
| Decision Date | March 01, 1988 |
| Days to Decision | 40 days |
| Submission Type | Traditional |
| Review Panel | Hematology (HE) |
| Summary | — |
| Product Code | JPK — Mixture, Hematology Quality Control |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 864.8625 |