K232677
- 510(k) number
- K232677
- Device name
- Reia pessary
- Applicant
- Reia, LLC NH · US
- Product code
- HHW — Pessary, Vaginal
- Decision date
- 2024-05-21
- Date received
- 2023-09-01
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Obstetrics/Gynecology
PDFDownload 510(k) SummaryArchived here · 0.5 MB · U.S. public domain
Also available from FDA: K232677.pdf
Official FDA record: K232677
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.