510(k) K230669 · LJS Catheter, Intravascular, Therapeutic, Long-Term Greater Than 30 Days
L-Cath Single and Dual Lumen Catheters, L-Cath Midline Catheters
| Applicant | Argon Medical Devices, Athens TX, US |
| Decision | Substantially Equivalent, Nov 30, 2023 |
| Received | Mar 10, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K230669
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Jul 24, 2026 | Argon Medical Devices, Inc L-Cath PICC S/L Peripherally Inserted Central Catheter: 26ga (1.9F) 0.60mm x 30cm, REF: 384539; 18ga (3.5F) 1.15mm x 60cm, REF: 384464; Basic Kit 28GA (1.2F) x 25cm 1 Lumen), REF: 384516; 20ga (3F) 1. Open, Classified |
LJS | None listed |
| Jul 24, 2026 | Argon Medical Devices, Inc L-Cath Midline S/L Catheter 20ga (3F) 1mm x 20cm, REF: 384620 Open, Classified |
LJS | None listed |
| Aug 16, 2024 | Argon Medical Devices, Inc L-CATH PICC S/L Peripherally Inserted Central Catheter, 26Ga (1.9F) 0.60mm x 30cm, REF: 384539 Open, Classified |
LJS | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.