Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K952794 |
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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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| Harvard 2 Dual Channel Syringe Infusion Pump P/N 2001-001 | 2 | 01/26/2005 |
FEI # 1218257 Harvard Clinical Technology |
| Software Versions V1.2R,or earlier for the Harvard 2, Dual Infusion Pump (P/N 2002-001) | 2 | 09/11/2003 |
FEI # 1218257 Harvard Clinical Technology |
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