Elvie Stride 2— 510(k) K242125
Substantially EquivalentChiaro Technology, Ltd.
FDA 510(k) clearance K242125 for Elvie Stride 2, Substantially Equivalent on 2024-09-27. Applicant: Chiaro Technology, Ltd..
Clearance details
- Applicant
- Chiaro Technology, Ltd.
- Product code
- Code HGX
- Advisory panel
- Obstetrics/Gynecology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Location
- London, GB
Adverse events under product code HGX
product code HGX- Injury
- 758
- Other
- 2
- Total
- 760
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.