Mosie Baby Kit— 510(k) K231203
Substantially EquivalentMosie Baby
FDA 510(k) clearance K231203 for Mosie Baby Kit, Substantially Equivalent on 2023-11-29. Applicant: Mosie Baby. Device class: 2.
Clearance details
- Applicant
- Mosie Baby
- Product code
- Code QYZ
- Device class
- Class 2
- Regulation
- 21 CFR 884.6110
- Advisory panel
- Obstetrics/Gynecology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Austin, TX, US
Recent devices under product code QYZ
view allData sourced from openFDA. This site is unofficial and independent of the FDA.