K232912
- 510(k) number
- K232912
- Device name
- Facet Aurora Reusable Lancet Base
- Applicant
- Facet Technologies, LLC GA · US
- Product code
- QRL — Multiple Use Blood Lancet For Single Patient Use Onl
- Decision date
- 2024-01-25
- Date received
- 2023-09-19
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General, Plastic Surgery
PDFDownload 510(k) SummaryArchived here · 3.0 MB · U.S. public domain
Also available from FDA: K232912.pdf
Official FDA record: K232912
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.