K241872
- 510(k) number
- K241872
- Device name
- Remanufactured EndoWrist ProGrasp Forceps (420093)
- Applicant
- Rebotix FL · US
- Product code
- QSM — System, Surgical, Computer Controlled Instrument, Re
- Decision date
- 2024-11-07
- Date received
- 2024-06-27
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Gastroenterology, Urology
PDFDownload 510(k) SummaryArchived here · 4.1 MB · U.S. public domain
Also available from FDA: K241872.pdf
Official FDA record: K241872
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.