K232633
- 510(k) number
- K232633
- Device name
- Gold Probe Bipolar Electrohemostasis Catheter; Injection Gold Probe Bipolar Electrohemostasis Catheter
- Applicant
- Boston Scientific MA · US
- Product code
- KNS — Unit, Electrosurgical, Endoscopic (With Or Without A
- Decision date
- 2023-11-28
- Date received
- 2023-08-30
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Gastroenterology, Urology
PDFDownload 510(k) SummaryArchived here · 1.1 MB · U.S. public domain
Also available from FDA: K232633.pdf
Official FDA record: K232633
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.