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Caphosol® Artifical Saliva (32 doses sachet box)
- Page Type
- Cleared 510(K)
- FDA Hosted PDF* The FDA doesn't provide PDFs for all submissions.
- 510(k) Number
- K234015
- 510(k) Type
- Traditional
- Applicant
- EUSA Pharma (UK) Limited
- Country
- United Kingdom
- FDA Decision
- Substantially Equivalent
- Decision Date
- 3/11/2024
- Days to Decision
- 83 days
- Submission Type
- Summary