# K200168: Dermapose Access

- Pathway: 510(k) (Traditional)
- Applicant: Puregraft, LLC
- Decided: Apr 22, 2020 after 90 days
- Product code: QPB (System, Suction, Lipoplasty For Removal)
- Device class: 2
- Regulation: 21 CFR 878.5040
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 5 generations back to K861878 (1986). 6 ancestors in all.
No later device cites it as a predicate yet.
0 of 7 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K142073: ST'RIM, Thiebaud Sas (2015) Summary page 5.

## Indications for use
The Dermapose Access fat harvest system is intended for use in aesthetic body contouring.

Source page: https://510kreport.com/device/K200168
Methodology: https://510kreport.com/methodology