Device, Percutaneous Retrieval
C.r. Bard, Inc.'s record for this product code
MDR events3All time
Recalls0All time
510(k) clearances1All time
Recent MDR events
3 adverse event reports on file
Recalls
0 recall events for this product code
No recalls on file for C.r. Bard, Inc. under this product code.
510(k) clearances
1 clearances for this product code