Medical Device Recalls
-
1 to 4 of 4 Results
510(K) Number: K102647 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
ENVOY 500 AST Reagent Kit, reference Model/Catalog 55255, for Envoy 500. Intended Use of the P... | 3 | 10/02/2014 | ELITech Clinical Systems SAS |
Viva-ProE Systems, Model # 6003-670, UDI: 03661540600357 - Product Usage: The ELITech Clinical Syst... | 3 | 09/30/2019 | ELITech Group B.V. |
Selectra ProM Analyzer, Catalog # 6003-435/UDI # 03661540600395 and Catalog # 6003-436/UDI # 0366154... | 2 | 10/16/2019 | Vital Scientific N.V. |
Selectra ProS Analyzer, Catalog # 6003-600/UDI # 03661540600418 Product Usage: :clinical chemist... | 2 | 10/16/2019 | Vital Scientific N.V. |
-