Medical Device Recalls
-
|
1 result found
510(K) Number: K895181 |
|
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| pO2 D999 membrane units. Distributed by Radiometer America, Inc., Westlake, OH 44145 pO2 membrane u... | 2 | 01/10/2014 | Radiometer America Inc |
-







