K895465 is an FDA 510(k) clearance for the AMDEV LYTENING 2Z SODIUM/POTASSIUM/LITHIUM ANALYZE. This device is classified as a Flame Photometry, Lithium (Class II - Special Controls, product code JIH).
Submitted by Baxter Healthcare Corp (Santa Ana, US). The FDA issued a Cleared decision on December 27, 1989, 107 days after receiving the submission on September 11, 1989.
This device falls under the Chemistry FDA review panel. Regulated under 21 CFR 862.3560.
| 510(k) Number | K895465 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | September 11, 1989 |
| Decision Date | December 27, 1989 |
| Days to Decision | 107 days |
| Submission Type | Traditional |
| Review Panel | Chemistry (CH) |
| Summary | — |
| Product Code | JIH — Flame Photometry, Lithium |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 862.3560 |