K232330
- 510(k) number
- K232330
- Device name
- Lancing System
- Applicant
- Ningbo Medsun Medical Co., Ltd. CN
- Product code
- QRK — Single Use Only Blood Lancet Without An Integral Sha
- Decision date
- 2024-01-04
- Date received
- 2023-08-03
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General, Plastic Surgery
PDFDownload 510(k) SummaryArchived here · 2.7 MB · U.S. public domain
Also available from FDA: K232330.pdf
Official FDA record: K232330
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.