K230841
- 510(k) number
- K230841
- Device name
- NailLift
- Applicant
- Jps Corporation JP
- Product code
- MQZ — Prosthesis, Nail
- Decision date
- 2024-01-22
- Date received
- 2023-03-28
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Unknown
PDFDownload 510(k) SummaryArchived here · 2.4 MB · U.S. public domain
Also available from FDA: K230841.pdf
Official FDA record: K230841
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.