Medical Device Recalls
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1 result found
510(K) Number: K090398 |
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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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Provent -SR - Sleep Apnea Therapy-SR (standard resistance). Prescription only, Single Use; Packed ... | 3 | 02/15/2012 | Ventus Medical, Inc. |
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