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U.S. Department of Health and Human Services

Medical Device Recalls
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510(K) Number: K150572
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Product Description
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Recall
Class
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FDA Recall
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Recalling Firm
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Respire Pink Series EF+ Oral Sleep Apnea Device. 2 05/29/2018 Respire Medical
Respire Pink+ Hard Oral Sleep Apnea Device 2 05/29/2018 Respire Medical
Respire Pink+ Hard/Soft Oral Sleep Apnea Device 2 05/29/2018 Respire Medical
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