K212969
- 510(k) number
- K212969
- Device name
- Liposaver
- Applicant
- Lhbiomed Co., Ltd. KR
- Product code
- QPB — System, Suction, Lipoplasty For Removal
- Decision date
- 2024-08-07
- Date received
- 2021-09-16
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General, Plastic Surgery
PDFDownload 510(k) SummaryArchived here · 0.8 MB · U.S. public domain
Also available from FDA: K212969.pdf
Official FDA record: K212969
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.