Medical Device Recalls
-
|
1 result found
510(K) Number: K014225 |
|
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| BreathTek Urea Hydrolysis Rate Calculation CD, Version 1.3.5 - January 1,'03, in vitro diagnostic. M... | 2 | 10/04/2007 | Meretek Diagnostics, Inc. |
-







