K250725

Hugo™ RAS System

510(k) number
K250725
Device name
Hugo™ RAS System
Applicant
Covidien, LLC CT · US
Product code
SCV — Modular Electromechanical Surgical System
Decision date
2025-12-03
Date received
2025-03-10
Decision
Substantially Equivalent
Clearance type
Traditional
Advisory committee
General, Plastic Surgery
PDFDownload 510(k) SummaryArchived here · 2.7 MB · U.S. public domain

Also available from FDA: K250725.pdf

Official FDA record: K250725
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.