Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K041499 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Aplio 50; SSA-700A; software version 5.5r002 | 2 | 03/19/2010 | Toshiba American Medical Systems Inc |
Aplio 80; SSA-770A; software version 5.5r002 | 2 | 03/19/2010 | Toshiba American Medical Systems Inc |
Toshiba Aplio 80 Digital Ultrasound System, SSA-770A with version 6 software | 2 | 06/27/2007 | Toshiba American Med Sys Inc |
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