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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