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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 3 of 3 Results
510(K) Number: K050751
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Product Description
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Recall
Class
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FDA Recall
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IMPAX® 4.1, IMPAX ® 4.5, IMPAX ® 5.0, IMPAX ® 5.1 IMPAX ® 5.2, IMPAX ® 6.0, IMPAX ® 6.2; Picture Arc... 2 09/11/2008 AGFA Corp.
WEB1000 Versions 3.1, 4.1 and 5.1, Picture Archiving and Communications systems (PACs), used in the ... 2 09/11/2008 AGFA Corp.
IMPAX® 6.2.1 System, Picture Archiving and Communications system (PAC), used in the acceptance, tran... 2 09/11/2008 AGFA Corp.
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