K241507
- 510(k) number
- K241507
- Device name
- ALN Optional Vena Cava Filter (FB.010500, FF.010995, FJ.120096, FB.HOOK, FF.HOOK, FJ.HOOK)
- Applicant
- Aln S.A.R.L. FR
- Product code
- DTK — Filter, Intravascular, Cardiovascular
- Decision date
- 2024-06-26
- Date received
- 2024-05-28
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Cardiovascular
PDFDownload 510(k) SummaryArchived here · 2.5 MB · U.S. public domain
Also available from FDA: K241507.pdf
Official FDA record: K241507
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.