K240359
- 510(k) number
- K240359
- Device name
- PowerGlide Pro Midline Catheter
- Applicant
- Becton, Dickinson and Company (Bard Access Systems, Inc.) UT · US
- Product code
- FOZ — Catheter, Intravascular, Therapeutic, Short-Term Les
- Decision date
- 2024-07-29
- Date received
- 2024-02-06
- 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: K240359.pdf
Official FDA record: K240359
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.