K241621
- 510(k) number
- K241621
- Device name
- Da Vinci Monopolar and Bipolar Adapters (378896)
- Applicant
- Intuitive Surgical CA · US
- Product code
- GEI — Electrosurgical, Cutting & Coagulation & Accessories
- Decision date
- 2024-08-02
- Date received
- 2024-06-05
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General, Plastic Surgery
PDFDownload 510(k) SummaryArchived here · 0.8 MB · U.S. public domain
Also available from FDA: K241621.pdf
Official FDA record: K241621
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.