Medical Device Recalls
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1 result found
510(K) Number: K982276 |
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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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(a) CareFusion Snowden-Pencer Plastics, Endoplastic Endoscope 10 mm, 30 degrees 7", 17.5 cm, Catalog... | 2 | 03/30/2022 | Carefusion 2200 Inc |
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