Medical Device Recalls
-
1 result found
510(K) Number: K102244 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
Reliance Endoscope Processing System (REPS), STERIS Corporation, 5960 Heisley Road, Mentor, OH 44060... | 2 | 09/20/2013 | Steris Corporation |
-