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510(k) K230669

L-Cath™ Single and Dual Lumen Catheters, L-Cath™ Midline Catheters by Argon Medical Devices — Product Code LJS

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 30, 2023
Date Received
March 10, 2023
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Catheter, Intravascular, Therapeutic, Long-Term Greater Than 30 Days
Device Class
Class II
Regulation Number
880.5970
Review Panel
HO
Submission Type

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Other clearances for product code LJS

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  • K243484 — PM2+ System and SmartPICC Stylet (May 29, 2025)
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