K250733
- 510(k) number
- K250733
- Device name
- 3DOSE 1ml Syringe
- Applicant
- Bimed Teknik Aletler Sanayi & Ticaret A.S. TR
- Product code
- FMF — Syringe, Piston
- Decision date
- 2025-07-03
- Date received
- 2025-03-11
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General Hospital
PDFDownload 510(k) SummaryArchived here · 0.4 MB · U.S. public domain
Also available from FDA: K250733.pdf
Official FDA record: K250733
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.