Remanufactured EndoWrist Cadiere Forceps (420049)— 510(k) K250399

Substantially Equivalent

Rebotix

FDA 510(k) clearance K250399 for Remanufactured EndoWrist Cadiere Forceps (420049), Substantially Equivalent on 2025-08-19. Applicant: Rebotix.

Clearance details

Applicant: Rebotix
Product code: Code QSM
Advisory panel: Gastroenterology, Urology
Date received: 2025-02-12
Decision date: 2025-08-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: St. Petersburg, FL, US

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