Cook Vandergrift Inc.DWSClass I

Instruments, Surgical, Cardiovascular

Cook Vandergrift Inc.'s record for this product code

MDR events3All time

Recalls1All time

510(k) clearances0All time

Recent MDR events

3 adverse event reports on file

Recalls

1 recall events for this product code

Open, ClassifiedSep 1, 2023
Sterility of device may be compromised due to breach of the chevron seal of the packaging
View FDA record ↗

510(k) clearances

0 clearances for this product code

No 510(k) clearances on file for Cook Vandergrift Inc. under this product code.