Medical Device Recalls
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1 to 5 of 5 Results
510(K) Number: K131855 |
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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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| Colonoscope Family # 1-Pentax Video Colonoscopes (EC Family) with One Instrument Channel and a Water... | 2 | 09/10/2021 |
FEI # 1000080301 Pentax of America Inc |
| Gastroscope Family # 1-Gastroscopes without a Water Jet Channel Models: EG-2790i, EG-1690K, EG-2490K... | 2 | 09/10/2021 |
FEI # 1000080301 Pentax of America Inc |
| Pentax Video Colonoscope Model: EC34-i10L | 2 | 02/19/2020 |
FEI # 1000080301 Pentax of America Inc |
| Pentax Video Colonoscope Model: EC38-i10L | 2 | 02/19/2020 |
FEI # 1000080301 Pentax of America Inc |
| Pentax Video Colonoscope is intended to be used with a PENTAX video processor (including light sourc... | 2 | 11/19/2016 |
FEI # 1000080301 Pentax of America Inc |
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