# System, Suction, Lipoplasty
> **Product code: MUU** · Class II — Moderate Risk (510(k) clearance required) · General, Plastic Surgery · 21 CFR 878.5040
## Classification
- **FDA Product Code:** MUU
- **Device class:** Class II — Moderate Risk (510(k) clearance required)
- **Regulation:** 21 CFR 878.5040
- **Review panel:** SU
- **Medical specialty:** General, Plastic Surgery
- **Submission type:** 1
- **GMP exempt:** N
- **Life sustaining:** N
- **Implant:** N
- **Third-party review:** N
## 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).

## Market data
- **Cleared 510(k) submissions:** 40
- **Registered establishments:** 41
## Source
- [FDA Device Classification](https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpcd/classification.cfm?ID=MUU)
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