Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K981446 |
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Product Description
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Recall
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FDA Recall
Posting Date |
Recalling Firm
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| Lp(a) Calibrator, Cat No. 998-41491, 1 ml glass bottles, in cardboard box, 2 bottles/box ,Waco Chemi... | 3 | 08/25/2006 |
FEI # 3005625991 Wako Chemicals, USA Inc |
| Wako Autokit Lp(a) Calibrator, model code# 998-41491, packaged in 1 ml bottles, 2 bottles/kit, and l... | 3 | 04/06/2012 |
FEI # 3005625991 Wako Chemicals USA, Inc. |
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