K242680
- 510(k) number
- K242680
- Device name
- LetsGetChecked Impress
- Applicant
- Privapath Diagnostics Ltd (Dba Letsgetchecked) IE
- Product code
- FMK — Single Use Only Blood Lancet With An Integral Sharps
- Decision date
- 2025-01-13
- Date received
- 2024-09-06
- Decision
- Unknown
- Clearance type
- Traditional
- Advisory committee
- General, Plastic Surgery
PDFDownload 510(k) SummaryArchived here · 0.8 MB · U.S. public domain
Also available from FDA: K242680.pdf
Official FDA record: K242680
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.