K250569 is an FDA 510(k) clearance for the Cardiologs Holter Platform. This device is classified as a Electrocardiograph (Class II - Special Controls, product code DPS).
Submitted by Philips France Commercial (Paris, FR). The FDA issued a Cleared decision on August 6, 2025, 161 days after receiving the submission on February 26, 2025.
This device falls under the Cardiovascular FDA review panel. Regulated under 21 CFR 870.2340.
| 510(k) Number | K250569 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | February 26, 2025 |
| Decision Date | August 06, 2025 |
| Days to Decision | 161 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 |