LifePath Remote Patient Monitoring Platform— 510(k) K211822
Substantially EquivalentElastic Care Incorporated
FDA 510(k) clearance K211822 for LifePath Remote Patient Monitoring Platform, Substantially Equivalent on 2022-02-03. Applicant: Elastic Care Incorporated.
Clearance details
- Applicant
- Elastic Care Incorporated
- Product code
- Code DRG
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Markham, CA
Recent devices under product code DRG
view allAdverse events under product code DRG
product code DRG- Death
- 5
- Total
- 5
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.