# K092195: Cutera Multimodal Cellulite Product (Cmmcd)

- Pathway: 510(k) (Special)
- Applicant: Cutera, Inc.
- Decided: Oct 1, 2009 after 72 days
- Product code: NUV (Massager, Vacuum, Light Induced Heating)
- Device class: 2
- Regulation: 21 CFR 878.4810
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 16 generations back to K943450 (1995). 103 ancestors in all.
No later device cites it as a predicate yet.
0 of 104 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K082622: Alma Lasers Accent B-Shape Massager Handpiece/Module, Alma Lasers, Ltd. (2009) Summary page 1.

## Indications for use
The Cutera CMMCD infrared(optional) and RF energies are intended to provide topical heating for the purpose of elevating tissue temperature for the treatment of selected medical conditions such as relief of pain, muscle spasms, and increase in local circulation. The Cutera CMMCD massage device is intended to provide a temporary reduction in the appearance of cellulite.

Source page: https://510kreport.com/device/K092195
Methodology: https://510kreport.com/methodology