K223788
- 510(k) number
- K223788
- Device name
- The MedSource TrueSafe Blood Control I.V. Safety Catheter, and the MedSource ClearSafe Blood Control I.V. Safety Catheter
- Applicant
- Medsource International, LLC MN · US
- Product code
- FOZ — Catheter, Intravascular, Therapeutic, Short-Term Les
- Decision date
- 2023-09-15
- Date received
- 2022-12-19
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General Hospital
PDFDownload 510(k) SummaryArchived here · 2.6 MB · U.S. public domain
Also available from FDA: K223788.pdf
Official FDA record: K223788
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.