K230669
- 510(k) number
- K230669
- Device name
- L-Cath Single and Dual Lumen Catheters, L-Cath Midline Catheters
- Applicant
- Argon Medical Devices TX · US
- Product code
- LJS — Catheter, Intravascular, Therapeutic, Long-Term Grea
- Decision date
- 2023-11-30
- Date received
- 2023-03-10
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General Hospital
510(k) Summary (official FDA PDF): K230669.pdf
Official FDA record: K230669
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.