K233106
- 510(k) number
- K233106
- Device name
- AccuCath Ace Intravascular Catheter
- Applicant
- Bard Access Systems, Inc. (C.R. Bard, Inc.) UT · US
- Product code
- FOZ — Catheter, Intravascular, Therapeutic, Short-Term Les
- Decision date
- 2024-04-19
- Date received
- 2023-09-27
- 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: K233106.pdf
Official FDA record: K233106
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.