Medical Device Recalls
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1 result found
510(K) Number: K090367 |
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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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Affected device is Model 98400-SL6-AHA, CardioExpress Electrocardiograph. The ECG cable part number ... | 2 | 01/13/2012 | Del Mar Reynolds Medical, Ltd. |
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