Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K000480 |
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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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| EM2 NC AEM Monitor (NON-COM) | 2 | 07/24/2003 |
FEI # 1000117361 Encision, Inc. |
| EM2+A NC AEM Monotor (NON-COM) | 2 | 07/24/2003 |
FEI # 1000117361 Encision, Inc. |
| EM2M NC AEM Monitor, (NON-COM) | 2 | 07/24/2003 |
FEI # 1000117361 Encision, Inc. |
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