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System, Suction, Lipoplasty

FDA product code MUU · 33 cleared devices

Class 2 General, Plastic Surgery
Regulation
21 CFR 878.5040
Review panel
SU
Implant
No
Life sustaining
No
Third party review
No
GMP exempt
No
Clearance span
2007-12-10 – 2022-03-16

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).

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