Medical Device Recalls
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1 result found
510(K) Number: K121463 |
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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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Phadia 1000 Instrument (introduced as UniCAP 1000), Article number: 12-3800-01 (All instrument softw... | 2 | 01/12/2015 | Phadia US Inc |
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