Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K951572 |
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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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Signmoidoscope Product Usage: Intended to provide optical visualization of, therapeutic access t... | 2 | 07/23/2016 | Pentax Medical Company |
Signmoidoscope Intended to provide optical visualization of, therapeutic access to, the Lower Gastr... | 2 | 06/28/2016 | Pentax Medical Company |
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