Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K112704 |
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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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LipiFlow Thermal Pulsation System/LipiFlow, System Activator (Disposable), Rx Only, Sterile | 2 | 03/22/2017 | Tearscience, Inc |
LipiFlow thermal Pulsation System, consisting of Console and Activator, Model LFD-1100 The LipiFl... | 2 | 10/17/2016 | Tearscience, Inc |
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