K922612 is an FDA 510(k) clearance for the CHOLESTECH LIPID MONITORING SYSTEM, TOTAL CHOLESTE. This device is classified as a Enzymatic Esterase--oxidase, Cholesterol (Class I - General Controls, product code CHH).
Submitted by Cholestech Corp. (Hayward, US). The FDA issued a Cleared decision on June 24, 1992, 22 days after receiving the submission on June 2, 1992.
This device falls under the Chemistry FDA review panel. Regulated under 21 CFR 862.1175.
| 510(k) Number | K922612 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | June 02, 1992 |
| Decision Date | June 24, 1992 |
| Days to Decision | 22 days |
| Submission Type | Traditional |
| Review Panel | Chemistry (CH) |
| Summary | Summary PDF |
| Product Code | CHH — Enzymatic Esterase--oxidase, Cholesterol |
| Device Class | Class I - General Controls |
| CFR Regulation | 21 CFR 862.1175 |