Medical Device Recalls
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1 result found
510(K) Number: K092713 |
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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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Spectre Wireless Footswitch/Handswitch system Model 98/99, Model FDS, Model FDB. The Spectre Wire... | 2 | 01/03/2014 | Trans American Medical, Inc. |
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