K260194
- 510(k) number
- K260194
- Device name
- Vacuum Pump (Model: AD-VPUM-500)
- Applicant
- Sheng Sheng Yi (Beijing) Technology Company Limited CN
- Product code
- MQG — Accessory, Assisted Reproduction
- Decision date
- 2026-04-28
- Date received
- 2026-01-22
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Obstetrics/Gynecology
PDFDownload 510(k) SummaryArchived here · 2.5 MB · U.S. public domain
Also available from FDA: K260194.pdf
Official FDA record: K260194
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.