K031557 is an FDA 510(k) clearance for the CARDIOVIT AT-102. This device is classified as a Electrocardiograph (Class II - Special Controls, product code DPS).
Submitted by Schiller AG (Baar, CH). The FDA issued a Cleared decision on April 14, 2004, 331 days after receiving the submission on May 19, 2003.
This device falls under the Cardiovascular FDA review panel. Regulated under 21 CFR 870.2340.
| 510(k) Number | K031557 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | May 19, 2003 |
| Decision Date | April 14, 2004 |
| Days to Decision | 331 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 |