Us Endovascular

FDA Regulatory Profile

Us Endovascular appears in FDA public data with 1 recall, 0 510(k) clearances, 1 FDA inspection, and 0 compliance actions on record. Its most recent recall (Z-1362-2016, Class II) was initiated on February 11, 2016.

Summary

Total Recalls
1
510(k) Clearances
0
Inspections
1
Compliance Actions
0

Recent Recalls

NumberClassProductDate
Z-1362-2016Class IIUSE (Ebony) PTA .014" rapid exchange (RX) Peripheral Dilatation Catheter. Distributed by US EndovasFebruary 11, 2016