FDA 510(k) Applications Submitted by PHILIPS MEDICAL SYSTEMS NETHERLAND, B.V.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K141979 | 07/21/2014 | ALLURA XPER FD SERIES / ALLURA XPER OR TABLE SERIES | PHILIPS MEDICAL SYSTEMS NETHERLAND, B.V. |
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