Medical Device Recalls
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1 result found
510(K) Number: K852544 |
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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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Kendall Monoject Syringe with Hypodermic Needle, 3cc syringe with 27 ga A-Bevel Needle (3cc- 27x1-1/... | 2 | 10/21/2006 | Kendall a Division of Tyco Healthcare Group LP |
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