Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K100125 |
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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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Product is a lithium ion battery sold as both a stand-alone accessory, and as part of endoscopy syst... | 2 | 01/29/2012 | Vision-Sciences, Inc. |
Product is a lithium ion battery charger sold as both a stand-alone accessory, and as part of endosc... | 2 | 01/29/2012 | Vision-Sciences, Inc. |
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