Milli Vaginal Dilator— 510(k) K211959
Substantially EquivalentMaterna Medical
FDA 510(k) clearance K211959 for Milli Vaginal Dilator, Substantially Equivalent on 2021-12-01. Applicant: Materna Medical.
Clearance details
- Applicant
- Materna Medical
- Product code
- Code HDX
- Advisory panel
- Obstetrics/Gynecology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mountain View, CA, US
Adverse events under product code HDX
product code HDX- Other
- 1
- Total
- 1
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.