Medical Device Recalls
-
1 result found
510(K) Number: K111182 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
AngioJet SOLENT Omni Thrombectomy Set: UPN 109681-004 & 109681-001, Catalog No 109681, Sterilized. ... | 2 | 08/13/2015 | Boston Scientific Corporation |
-