FDA 510(k) Applications Submitted by Maria Keelan
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K061675 | 06/14/2006 | VISION VXC CENTRAL STATION, MODEL 4300 | INVIVO CORPORATION |
| K212227 | 07/16/2021 | Philips MR Patient Care Portal | Invivo Corporation |
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