Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K013596 |
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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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VerifyNow IIb/IIIa Test, 10-Test Kit, Catalog No. 85310, 10 tests/box; 690 total tests. The Ve... | 2 | 12/11/2013 | Accumetrics Inc |
VerifyNow IIb/IIIa Test, Catalog No. 85310, 10-Test Kit and Catalog No. 85011, 25-Test kit. Produ... | 2 | 03/11/2014 | Accumetrics Inc |
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