K241810
- 510(k) number
- K241810
- Device name
- MICROLET®NEXT Lancet
- Applicant
- Ascensia Diabetes Care U.S., Inc. NJ · US
- Product code
- QRK — Single Use Only Blood Lancet Without An Integral Sha
- Decision date
- 2024-08-15
- Date received
- 2024-06-21
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General, Plastic Surgery
PDFDownload 510(k) SummaryArchived here · 0.5 MB · U.S. public domain
Also available from FDA: K241810.pdf
Official FDA record: K241810
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.