K243807
- 510(k) number
- K243807
- Device name
- Single Use Retrieval Basket V FG-V421PR/V422PR/V431P/V432P
- Applicant
- Olympus Medical Systems Corp. JP
- Product code
- LQR — Dislodger, Stone, Biliary
- Decision date
- 2025-03-18
- Date received
- 2024-12-11
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Gastroenterology, Urology
PDFDownload 510(k) SummaryArchived here · 0.6 MB · U.S. public domain
Also available from FDA: K243807.pdf
Official FDA record: K243807
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.