Medical Device Recalls
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1 result found
510(K) Number: K983519 |
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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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Sea-Clens Wound Cleanser, 6 fl. oz., Manufactured by Coloplast Corp., Marietta, GA, #11701-159-36, ... | 2 | 04/04/2007 | Coloplast Corp Skin Care Div |
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