ST'RIM

System, Suction, Lipoplasty

THIEBAUD SAS

The following data is part of a premarket notification filed by Thiebaud Sas with the FDA for St'rim.

Pre-market Notification Details

• Device ID: K142073
• 510k Number: K142073
• Device Name: ST'RIM
• Classification: System, Suction, Lipoplasty
• Applicant: THIEBAUD SAS 5600 WISCONSIN AVE, #509 Chevy Chase, MD 20815
• Contact: Patsy J Trisler, Jd, Rac
• Correspondent: Patsy J Trisler, Jd, Rac; THIEBAUD SAS 5600 WISCONSIN AVE, #509 Chevy Chase, MD 20815
• Product Code: MUU
• CFR Regulation Number: 878.5040 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 2014-07-31
• Decision Date: 2015-04-29
• Summary: summary