Isovac Products, LLC is one of 18215 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Isovac Products, LLC - FDA 510(k) Cleared Devices
Recent clearances: ORCA (tm) - Operational Rescue Containment Apparatus, CAPSULS, MODELS 2003-PUR8C, 2004-PVC8C
2
Total
2
Cleared
0
Denied
Isovac Products, LLC has 2 FDA 510(k) cleared medical devices. Based in Bellaire, US.
Historical record: 2 cleared submissions from 2006 to 2017. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Isovac Products, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Jl Jones Group, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Isovac Products, LLC
2 devices