FDA 510(k) Applications Submitted by Peter Mortier
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K223855 | 12/23/2022 | FEops HEARTguideTM, FEops HEARTguideTM ALPACA | FEops nv |
| K214066 | 12/27/2021 | FEops HEARTguide | FEops nv |
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