K791159 is an FDA 510(k) clearance for the DINAMAP MODEL 855. This device is classified as a System, Measurement, Blood-pressure, Non-invasive (Class II - Special Controls, product code DXN).
Submitted by Applied Medical Research (Mchenry, US). The FDA issued a Cleared decision on July 30, 1979, 39 days after receiving the submission on June 21, 1979.
This device falls under the Cardiovascular FDA review panel. Regulated under 21 CFR 870.1130.
| 510(k) Number | K791159 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | June 21, 1979 |
| Decision Date | July 30, 1979 |
| Days to Decision | 39 days |
| Submission Type | Traditional |
| Review Panel | Cardiovascular (CV) |
| Summary | — |
| Product Code | DXN — System, Measurement, Blood-pressure, Non-invasive |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 870.1130 |