Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K002028 |
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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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| Medtronic Bravo pH Capsule with Delivery System, Stomach pH electrode, Product Numbers 9012B1011 and... | 2 | 05/07/2008 |
FEI # 2182207 Medtronic Neuromodulation |
| Given Imaging Bravo®® pH capsule delivery device, 1-pack. In- Vitor Diagnostic for pH monitoring of... | 2 | 05/06/2016 |
FEI # 1219930 Covidien LLC |
| Given Imaging Bravo® pH capsule delivery device, 5-pack. In-Vitro Diagnostic for pH monitoring of g... | 2 | 05/06/2016 |
FEI # 1219930 Covidien LLC |
| Bravo pH Monitoring System Receiver | 3 | 07/20/2004 |
FEI # 1000135098 Medtronic Gastroenterology / Urology |
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