K242388
- 510(k) number
- K242388
- Device name
- LensHooke X12 PRO Semen Analysis System
- Applicant
- Bonraybio Co., Ltd. TW
- Product code
- POV — Semen Analysis Device
- Decision date
- 2025-05-09
- Date received
- 2024-08-12
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Hematology
PDFDownload 510(k) SummaryArchived here · 2.9 MB · U.S. public domain
Also available from FDA: K242388.pdf
Official FDA record: K242388
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.