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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 9 of 9 Results
510(K) Number: K072847
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Product Description
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Hologic QDR 4500 series Bone Densitometer Software versions 12.6, 2.3., or 2.4 Indicated for the... 2 08/25/2009 Hologic, Inc.
Hologic Explorer series Bone Densitometer System Software versions 12.6, 2.3., or 2.4. Indicate... 2 08/25/2009 Hologic, Inc.
Hologic Discovery series Bone Densitometer System Software versions 12.6, 2.3., or 2.4. Indicat... 2 08/25/2009 Hologic, Inc.
Hologic Delphi series Bone Densitometer Software versions 12.6, 2.3., or 2.4 Indicated for the e... 2 08/25/2009 Hologic, Inc.
Hologic Explorer Bone Densitometers with Apex software versions 2.0, 2.1 and 2.2 is indicated for t... 2 09/17/2008 Hologic, Inc.
Hologic Delphi Bone Densitometers with Apex software versions 2.0, 2.1 and 2.2 is indicated for the... 2 09/17/2008 Hologic, Inc.
Hologic QDR4500 Bone Densitometers with Apex software versions 2.0, 2.1 and 2.2 is indicated for t... 2 09/17/2008 Hologic, Inc.
Hologic Discovery Bone Densitometers with Apex software versions 2.0, 2.1 and 2.2 is indicated for ... 2 09/17/2008 Hologic, Inc.
Hologic Oasis Bone Densitometers with Apex software versions 2.0, 2.1 and 2.2 is indicated for the e... 2 09/17/2008 Hologic, Inc.
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