K261706
- 510(k) number
- K261706
- Device name
- Endomat Select (UP220)
- Applicant
- KARL STORZ SE & CO. KG DE
- Product code
- HIG — Insufflator, Hysteroscopic
- Decision date
- 2026-07-16
- Date received
- 2026-05-22
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Obstetrics/Gynecology
PDFDownload 510(k) SummaryArchived here · 0.6 MB · U.S. public domain
Also available from FDA: K261706.pdf
Official FDA record: K261706
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.