Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K973662 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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ACCU-CHEK Complete blood glucose monitor, Ref. no. 516; Catalog nos. 03266770001 and 03871983001 wit... | 2 | 08/05/2006 | Roche Diagnostics Corp. |
ACCU-CHEK Complete diabetes monitoring kit/ care kit/ insulin pump therapy kit, Cat. no 515; Ref. no... | 2 | 08/05/2006 | Roche Diagnostics Corp. |
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