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. Device class: 2.
Clearance details
- Applicant
- Rebotix
- Product code
- Code QSM
- Device class
- Class 2
- Regulation
- 21 CFR 876.1500
- Advisory panel
- Gastroenterology, Urology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- St. Petersburg, FL, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.