MUU

System, Suction, Lipoplasty

Product code

MUU

Device name

System, Suction, Lipoplasty

Device class

Class 2

21 CFR

21 CFR 878.5040

Medical specialty

General, Plastic Surgery

Marketing pathway

510(K)

510(k) clearances (all years, FDA)

40 (all years; only the last 3 years are listed here)

FDA classification definition

See Federal Register Notice at 86 FR 50887 “Consolidation of Devices That Process Autologous Human Cells, Tissues, and Cellular and Tissue-Based Products at the Point of Care to Produce a Therapeutic Article” (FRN) (FDA-2021-N-0881).

Definition text from the FDA device classification database (U.S. federal government work, public domain).