K822972 is an FDA 510(k) clearance for the IL 801 THERMALDILUTION CARDIAC OUTPUT. This device is classified as a Computer, Diagnostic, Pre-programmed, Single-function (Class II - Special Controls, product code DXG).
Submitted by Instrumentation Laboratory CO (Mchenry, US). The FDA issued a Cleared decision on November 1, 1982, 24 days after receiving the submission on October 8, 1982.
This device falls under the Cardiovascular FDA review panel. Regulated under 21 CFR 870.1435.
| 510(k) Number | K822972 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | October 08, 1982 |
| Decision Date | November 01, 1982 |
| Days to Decision | 24 days |
| Submission Type | Traditional |
| Review Panel | Cardiovascular (CV) |
| Summary | — |
| Product Code | DXG — Computer, Diagnostic, Pre-programmed, Single-function |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 870.1435 |