K231724
- 510(k) number
- K231724
- Device name
- Flush Syringe (Prefilled 0.9% normal saline solution)
- Applicant
- Spm Medicare Pvt. , Ltd. IN
- Product code
- NGT — Saline, Vascular Access Flush
- Decision date
- 2023-11-09
- Date received
- 2023-06-13
- 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: K231724.pdf
Official FDA record: K231724
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.