K253235
- 510(k) number
- K253235
- Device name
- Introcan Safety® Deep Access XL IV Catheter
- Applicant
- B.Braun Medical, Inc. PA · US
- Product code
- FOZ — Catheter, Intravascular, Therapeutic, Short-Term Les
- Decision date
- 2026-05-15
- Date received
- 2025-09-29
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General Hospital
PDFDownload 510(k) SummaryArchived here · 2.7 MB · U.S. public domain
Also available from FDA: K253235.pdf
Official FDA record: K253235
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.