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FDA 510(k) Applications Submitted by NANDINI MURPHY
FDA 510(k) Number
Submission Date
Device Name
Applicant
K983028
08/31/1998
FRACTURE RISK OPTION FOR THE QDR BONE DENSITOMETER, MODEL#S QDR4500, QDR2000, QDR1500, QDR4000, QDR1000, QDR1000W
HOLOGIC, INC.
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