Cardiologs Holter Platform— 510(k) K250569
Substantially EquivalentPhilips France Commercial
FDA 510(k) clearance K250569 for Cardiologs Holter Platform, Substantially Equivalent on 2025-08-06. Applicant: Philips France Commercial.
Clearance details
- Applicant
- Philips France Commercial
- Product code
- Code DPS
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Paris, FR
Adverse events under product code DPS
product code DPS- Death
- 7
- Total
- 7
Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →
Data sourced from openFDA. This site is unofficial and independent of the FDA.