Medical Device Recalls
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1 result found
510(K) Number: K102047 |
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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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Innocor Cardiopulmonary Exercise and Lung Function Testing System Non-invasive diagnostic devic... | 2 | 09/08/2016 | Innovision A/S |
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