Medical Device Recalls
-
1 to 4 of 4 Results
510(K) Number: K883718 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
Pressure Monitoring Tubing, PM6006. Pressure Monitoring Tubing (PM series) is used between the man... | 2 | 04/03/2014 | Merit Medical Systems, Inc. |
Custom Angiographic Kit | 2 | 03/06/2003 | Merit Medical Systems, Inc |
Custom Angiographic Kit. | 2 | 03/06/2003 | Merit Medical Systems, Inc |
Custom Angiographic Kit | 2 | 03/06/2003 | Merit Medical Systems, Inc |
-