SENTIO MMG Gen 2— 510(k) K173526

Substantially Equivalent

Medos International SARL

FDA 510(k) clearance K173526 for SENTIO MMG Gen 2, Substantially Equivalent on 2018-04-05. Applicant: Medos International SARL. Device class: 2.

Clearance details

Applicant
Medos International SARL
Product code
Code PDQ
Device class
Class 2
Regulation
21 CFR 874.1820
Advisory panel
Ear, Nose, Throat
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Lelocle, CH
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