Medical Device Recalls
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1 result found
510(K) Number: K946258 |
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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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Advanced Orthogonal Percussion Adjusting Instrument Indicated for use by a licensed Chiropractor... | 2 | 07/25/2013 | Advanced Orthogonal Equipment, Incorporated |
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