K233794
- 510(k) number
- K233794
- Device name
- Insulin Syringe
- Applicant
- Spm Medicare Pvt. , Ltd. IN
- Product code
- FMF — Syringe, Piston
- Decision date
- 2024-03-06
- Date received
- 2023-11-28
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Flag
- Third-party review
- Advisory committee
- General Hospital
PDFDownload 510(k) SummaryArchived here · 2.6 MB · U.S. public domain
Also available from FDA: K233794.pdf
Official FDA record: K233794
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.