Medical Device Recalls
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1 result found
510(K) Number: K972220 |
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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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Rheumatoid Factor Standard (RF CAL) Catalogue Number: RF2301 GTIN: 05055273205039 Product Usage:... | 2 | 11/04/2019 | Randox Laboratories Ltd. |
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