K223826
- 510(k) number
- K223826
- Device name
- NanoDrop Lancet
- Applicant
- Drawbridge Health, Inc. FL · US
- Product code
- FMK — Single Use Only Blood Lancet With An Integral Sharps
- Decision date
- 2024-02-22
- Date received
- 2022-12-21
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General, Plastic Surgery
PDFDownload 510(k) SummaryArchived here · 2.6 MB · U.S. public domain
Also available from FDA: K223826.pdf
Official FDA record: K223826
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.