Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K963056 |
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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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Video Duodenoscope These instruments are intended to provide optical visualization of (via a vide... | 2 | 07/11/2017 | Pentax of America Inc |
Duodenoscope Product Usage: Intended to provide optical visualization of and therapeutic access ... | 2 | 07/23/2016 | Pentax Medical Company |
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