Medical Device Recalls
-
1 result found
510(K) Number: K920156 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
MoniTorr 10100 10-100 CSF Drainage System w/Patient Line One Way Valve MoniTorr 10102 10-102 CSF Dr... | 1 | 05/20/2019 | Integra LifeSciences Corp. |
-