FDA 510(k) Applications Submitted by SCOTT BISHOP

FDA 510(k) Number Submission Date Device Name Applicant
K230669 03/10/2023 L-CathÖ Single and Dual Lumen Catheters, L-CathÖ Midline Catheters Argon Medical Devices
K061758 06/22/2006 ACTIVE RENIN IRMA DIAGNOSTIC SYSTEMS LABORATORIES, INC.
K242612 09/03/2024 Option ELITE Vena Cava Filter System (352506070E 352506100E) Argon Medical Devices, Inc.
K213002 09/20/2021 SCORPION Portal Vein Access Set Argon Medical Devices


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