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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ARCHITECT i2000SR Processing Module, for in vitro diagnostics, List Number 3M74-01; manufactured by ... | 2 | 05/09/2007 | Abbott Laboratories, Inc |
ARCHITECT i2000sr Processing Module, for in vitro diagnostics; List Number 3M74-01; v2.10, v2.11, v2... | 2 | 06/19/2007 | Abbott Laboratories, Inc |
ARCHTECT System RS-232 Manual, product list number 06F71-04, for the ARCHITECT i2000 Processing Modu... | 3 | 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 |
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