Remanufactured EndoWrist ProGrasp Forceps (420093)— 510(k) K241872
Substantially EquivalentRebotix
FDA 510(k) clearance K241872 for Remanufactured EndoWrist ProGrasp Forceps (420093), Substantially Equivalent on 2024-11-07. Applicant: Rebotix.
Clearance details
- Applicant
- Rebotix
- Product code
- Code QSM
- Advisory panel
- Gastroenterology, Urology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- St. Petersburg, FL, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.