K241731
- 510(k) number
- K241731
- Device name
- Outlook Surgical Versa One System (8900139)
- Applicant
- Resnent, LLC IL · US
- Product code
- EOB — Nasopharyngoscope (Flexible Or Rigid)
- Decision date
- 2025-08-11
- Date received
- 2024-06-17
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Ear, Nose, Throat
PDFDownload 510(k) SummaryArchived here · 0.5 MB · U.S. public domain
Also available from FDA: K241731.pdf
Official FDA record: K241731
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.