Suction Lipoplasty System

System, Suction, Lipoplasty


The following data is part of a premarket notification filed by Thiebaud Sas with the FDA for Suction Lipoplasty System.

Pre-market Notification Details

Device IDBK220750
510k NumberBK220750
Device Name:Suction Lipoplasty System
ClassificationSystem, Suction, Lipoplasty
Applicant THIEBAUD SAS 2 Impasse Des Primbois Margencel,  Haute-Savoie,  74200,  FRANCE
Product CodeMUU  
CFR Regulation Number878.5040 [🔎]
DecisionSubstantially Equivalent (SE)
Type510(k) Special
3rd Party ReviewedNo
Combination ProductNo
Date Received2022-07-28
Decision Date2022-08-26

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