K233069
- 510(k) number
- K233069
- Device name
- Removal System Large Bore 60 cc Syringe
- Applicant
- Inari Medical, Inc. CA · US
- Product code
- PUR — Vacuum Syringe
- Decision date
- 2024-03-26
- Date received
- 2023-09-26
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General Hospital
PDFDownload 510(k) SummaryArchived here · 0.9 MB · U.S. public domain
Also available from FDA: K233069.pdf
Official FDA record: K233069
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.