Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K862649 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| MicroVue CIC-C1q EIA, Model A001. The MicroVue CIC-C1q EIA is for detection of circulating immune co... | 3 | 04/24/2018 |
FEI # 1000122536 Diagnostic Hybrids, Inc. |
| MicroVue CIC-C1q EIA, Model A001. An enzyme immunoassay for the detection of circulating immune com... | 2 | 04/24/2018 |
FEI # 1000122536 Diagnostic Hybrids, Inc. |
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