K791778 is an FDA 510(k) clearance for the MEDTRONIC MODEL 9410 TELETRACE RECEIVER. This device is classified as a Transmitters And Receivers, Electrocardiograph, Telephone (Class II - Special Controls, product code DXH).
Submitted by Medtronic Vascular (Walker, US). The FDA issued a Cleared decision on October 2, 1979, 22 days after receiving the submission on September 10, 1979.
This device falls under the Cardiovascular FDA review panel. Regulated under 21 CFR 870.2920.
| 510(k) Number | K791778 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | September 10, 1979 |
| Decision Date | October 02, 1979 |
| Days to Decision | 22 days |
| Submission Type | Traditional |
| Review Panel | Cardiovascular (CV) |
| Summary | — |
| Product Code | DXH — Transmitters And Receivers, Electrocardiograph, Telephone |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 870.2920 |