Medical Device Recalls
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1 result found
510(K) Number: K130178 |
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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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Inspiration Ventilator System, i Series and LS 12.1 LCD. The Inspiration 7i / 5i Ventilator Syste... | 1 | 11/19/2015 | Event Medical LTD |
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