Medical Device Recalls
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1 result found
510(K) Number: K051476 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Model 73X Uni-Vent Product Usage: Intended for use at mass casualty incidents. | 2 | 06/26/2015 | Impact Instrumentation, Inc. |
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