K240192
- 510(k) number
- K240192
- Device name
- Single-use Extraction Baskets
- Applicant
- Scivita Medical Technology Co., Ltd. CN
- Product code
- LQR — Dislodger, Stone, Biliary
- Decision date
- 2024-10-15
- Date received
- 2024-01-24
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Gastroenterology, Urology
PDFDownload 510(k) SummaryArchived here · 1.0 MB · U.S. public domain
Also available from FDA: K240192.pdf
Official FDA record: K240192
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.