K251687
- 510(k) number
- K251687
- Device name
- Konig Bell Circumcision Clamp
- Applicant
- Medline Industries, LP IL · US
- Product code
- HFX — Clamp, Circumcision
- Decision date
- 2026-02-25
- Date received
- 2025-06-02
- 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: K251687.pdf
Official FDA record: K251687
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.