K231203
- 510(k) number
- K231203
- Device name
- Mosie Baby Kit
- Applicant
- Mosie Baby TX · US
- Product code
- QYZ — At Home Intravaginal Insemination System
- Decision date
- 2023-11-29
- Date received
- 2023-04-27
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Obstetrics/Gynecology
PDFDownload 510(k) SummaryArchived here · 0.0 MB · U.S. public domain
Also available from FDA: K231203.pdf
Official FDA record: K231203
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.