K253602
- 510(k) number
- K253602
- Device name
- Precision S 4K Sinuscope
- Applicant
- Stryker Endoscopy CA · US
- Product code
- GWG — Endoscope, Neurological
- Decision date
- 2026-06-04
- Date received
- 2025-11-18
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Neurology
PDFDownload 510(k) SummaryArchived here · 0.9 MB · U.S. public domain
Also available from FDA: K253602.pdf
Official FDA record: K253602
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.