Medical Device Recalls
-
|
1 to 4 of 4 Results
510(K) Number: K062925 |
|
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| Roche Coaguchex XS Systems for Patient Self-Testing, Roche Diagnostics, Indianapolis, IN; REF 048377... | 2 | 08/11/2009 |
FEI # 1823260 Roche Diagnostics Corp. |
| CoaguChek XS PST Meters- IVD (Patient Self-Testing) measures blood-clotting time for people who are ... | 2 | 01/07/2021 |
FEI # 1823260 Roche Diagnostics Operations, Inc. |
| CoaguChek XS System (PST) The CoaguChek XS PT test strips are part of the CoaguChek XS System. Th... | 2 | 06/24/2013 |
FEI # 1823260 Roche Diagnostics Operations, Inc. |
| Roche CoaguChek XS System, CoaguChek XS PST Kit, Roche Diagnostics, Indianapolis, IN; Catalog/Model ... | 2 | 09/03/2009 |
FEI # 1823260 Roche Diagnostics Operations, inc. |
-







