Portavision Medical, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Portavision Medical, LLC - FDA 510(k) Cleared Devices
Recent clearances: Virtual C DRF-NEO Digital Imaging System, Virtual C DRF Digital Imaging System, MobileRay Pulse SE Digital Imaging System
5
Total
5
Cleared
0
Denied
Portavision Medical, LLC has 5 FDA 510(k) cleared medical devices. Based in Kenner, US.
Last cleared in 2021. Active since 2008. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Portavision Medical, LLC Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Kamm & Associates and Kamm and Associates.
FDA 510(k) Regulatory Record - Portavision Medical, LLC
5 devices
Cleared
Sep 24, 2021
Virtual C DRF-NEO Digital Imaging System
Radiology
42d
Cleared
Jun 24, 2021
Virtual C DRF Digital Imaging System
Radiology
64d
Cleared
Sep 04, 2019
MobileRay Pulse SE Digital Imaging System
Radiology
90d
Cleared
Apr 16, 2014
PVMED DDR 2430T
Radiology
152d
Cleared
Nov 21, 2008
NEORAY DR 2520 DIGITAL IMAGING SYSTEM
Radiology
38d