Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K982928 |
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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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| Dri-Tek BG-OX Cartridge, Model #D7120, Cat. #946-003 Cartridges used in the NPT7 Analyzer, an in vit... | 2 | 07/27/2006 |
FEI # 1523456 Radiometer America Inc |
| D7120, BG-OX Cartridge, D7120 REF 946-003, and 946-001, cuvettes for the NPT7 series of blood gas an... | 3 | 08/26/2006 |
FEI # 1523456 Radiometer America Inc |
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