Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K951199 |
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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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Bronchoscope Intended to provide optical visualization of and therapeutic access to the Airway and ... | 2 | 06/28/2016 | Pentax Medical Company |
Ultrasound Bronchoscope Intended to provide optical visualization of, ultrasonic visualization of a... | 2 | 06/28/2016 | Pentax Medical Company |
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