Medical Device Recalls
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11 to 14 of 14 Results
510(K) Number: K983212 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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ARCHTECT System RS-232 Manual, product list number 06F71-04, for the ARCHITECT i2000 Processing Modu... | 3 | 07/20/2004 | Abbott Laboratories, Inc |
ARCHITECT Processing Module, manufactured by Abbott Laboratories, Irving, Texas | 2 | 07/20/2004 | Abbott Laboratories, Inc |
The ARCHITECT i2000, Clinical Chemistry Analyzer, Manufactured by Abbott Laboratories, Irving, Texas | 2 | 12/24/2003 | Abbott Laboratories, Inc |
ARCHITECT Processing Module, List number 8C89-01, manufactured by Abbott Laboratories, Irving, Texas | 2 | 08/13/2003 | Abbott Laboratories, Inc |
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