Last synced on 30 May 2025 at 11:05 pm

L-Cath™ Single and Dual Lumen Catheters, L-Cath™ Midline Catheters

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K230669
510(k) Type
Traditional
Applicant
Argon Medical Devices
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/30/2023
Days to Decision
265 days
Submission Type
Summary

L-Cath™ Single and Dual Lumen Catheters, L-Cath™ Midline Catheters

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K230669
510(k) Type
Traditional
Applicant
Argon Medical Devices
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/30/2023
Days to Decision
265 days
Submission Type
Summary