K231242
- 510(k) number
- K231242
- Device name
- Perifix FX Catheter; Contiplex FX Catheter
- Applicant
- B.Braun Medical, Inc. PA · US
- Product code
- BSO — Catheter, Conduction, Anesthetic
- Decision date
- 2023-09-15
- Date received
- 2023-05-01
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Anesthesiology
PDFDownload 510(k) SummaryArchived here · 0.4 MB · U.S. public domain
Also available from FDA: K231242.pdf
Official FDA record: K231242
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.