K241842
- 510(k) number
- K241842
- Device name
- Luer-Split MAJ-2092
- Applicant
- Olympus Medical Systems Corporation JP
- Product code
- ODC — Endoscope Channel Accessory
- Decision date
- 2025-03-19
- Date received
- 2024-06-26
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Gastroenterology, Urology
PDFDownload 510(k) SummaryArchived here · 0.8 MB · U.S. public domain
Also available from FDA: K241842.pdf
Official FDA record: K241842
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.