Medical Device Recalls
-
1 result found
510(K) Number: K072929 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
LimiTorr INS9020 INS-9020 LIMITORR VOLUME LIMITING EVD 20 ML LimiTorr INS9020SP1 INS-9020SP1 LIMITO... | 1 | 05/20/2019 | Integra LifeSciences Corp. |
-