The following data is part of a premarket notification filed by Thiebaud Sas with the FDA for Suction Lipoplasty System.
| Device ID | BK220750 |
| 510k Number | BK220750 |
| Device Name: | Suction Lipoplasty System |
| Classification | System, Suction, Lipoplasty |
| Applicant | THIEBAUD SAS 2 Impasse Des Primbois Margencel, Haute-Savoie, 74200, FRANCE |
| Product Code | MUU |
| CFR Regulation Number | 878.5040 [🔎] |
| Decision | Substantially Equivalent (SE) |
| Type | 510(k) Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2022-07-28 |
| Decision Date | 2022-08-26 |