K241874
- 510(k) number
- K241874
- Device name
- Aspiration Catheter (2189)
- Applicant
- Hobbs Medical, Inc. CT · US
- Product code
- OCX — Endoscopic Irrigation/Suction System
- Decision date
- 2024-09-24
- Date received
- 2024-06-28
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Gastroenterology, Urology
PDFDownload 510(k) SummaryArchived here · 0.3 MB · U.S. public domain
Also available from FDA: K241874.pdf
Official FDA record: K241874
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.