Medical Device Recalls
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1 result found
510(K) Number: K890718 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Remel QC-Slide Gram Stain Control, Catalog #40142, packaged 45/box. The responsible firm on the lab... | 2 | 12/25/2003 | Remel, Inc. |
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