Medical Device Recalls
-
1 result found
510(K) Number: K092407 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
Remel Spectra MRSA, Ref R01821, 10 plates per package, and Ref R01822, 100 plates per package. The ... | 2 | 06/28/2011 | Remel Inc |
-