Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K131902 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Pentax Video Gastroscope is intended to be used with a Pentax video processor (including light sourc... | 2 | 10/26/2016 | Pentax of America Inc |
| Gastroscope Intended to provide optical visualization of and therapeutic access to the Upper Gastro... | 2 | 06/28/2016 | Pentax Medical Company |
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