Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K961564 |
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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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Gastroscope Intended to provide optical visualization of and therapeutic access to the Upper Gastro... | 2 | 06/28/2016 | Pentax Medical Company |
EE- Series Video Esophagoscopes, EE-1580K. Intended to provide optical visualization of (via a vi... | 2 | 01/20/2012 | Pentax Medical Company |
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