K964784 is an FDA 510(k) clearance for the SYNERGY CARDIOLOGY INFORMATION SYSTEM (00431). This device is classified as a Electrocardiograph (Class II - Special Controls, product code DPS).
Submitted by Quinton, Inc. (Bothell, US). The FDA issued a Cleared decision on August 13, 1997, 259 days after receiving the submission on November 27, 1996.
This device falls under the Cardiovascular FDA review panel. Regulated under 21 CFR 870.2340.
| 510(k) Number | K964784 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | November 27, 1996 |
| Decision Date | August 13, 1997 |
| Days to Decision | 259 days |
| Submission Type | Traditional |
| Review Panel | Cardiovascular (CV) |
| Summary | Summary PDF |
| Product Code | DPS — Electrocardiograph |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 870.2340 |