K234015
- 510(k) number
- K234015
- Device name
- Caphosol® Artifical Saliva (32 doses sachet box)
- Applicant
- Eusa Pharma (Uk) Limited GB
- Product code
- LFD — Saliva, Artificial
- Decision date
- 2024-03-11
- Date received
- 2023-12-19
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Unknown
PDFDownload 510(k) SummaryArchived here · 2.1 MB · U.S. public domain
Also available from FDA: K234015.pdf
Official FDA record: K234015
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.