Medical Device Recalls
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1 result found
510(K) Number: K002763 |
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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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RemRest Non-Invasive Continuous Positive Airway Pressure System, Model 903. The firm name on the de... | 2 | 12/17/2004 | Medical Industries America Inc |
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