Medical Device Recalls
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1 result found
510(K) Number: K112220 |
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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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DeVilbiss Model DV5x Series CPAP units. For use in treating Obstructive Sleep Apnea (OSA) by means o... | 3 | 07/01/2014 | DeVilbiss Healthcare LLC |
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