Medical Device Recalls
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1 result found
510(K) Number: K023318 |
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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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ON-Q pump with ONDEMAND bolus button, ON-Q C-bloc with ONDEMAND; ON-Q C-bloc with Select a Flow and ... | 1 | 08/28/2012 | I-Flow Corporation |
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