K233623
- 510(k) number
- K233623
- Device name
- Praxiject SP 0.9% NaCl
- Applicant
- Medxl, Inc. CA
- Product code
- NGT — Saline, Vascular Access Flush
- Decision date
- 2024-02-27
- Date received
- 2023-11-13
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General Hospital
PDFDownload 510(k) SummaryArchived here · 0.5 MB · U.S. public domain
Also available from FDA: K233623.pdf
Official FDA record: K233623
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.