Medical Device Recalls
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1 result found
510(K) Number: K080983 |
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Product Description
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Recall
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FDA Recall
Posting Date |
Recalling Firm
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| The Provent Nasal Cannula is a nasal appliance device placed in both nostrils intended to be used fo... | 3 | 09/19/2010 |
FEI # 3007038487 Ventus Medical, Inc. |
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