FDA 510(k) Applications Submitted by Sarah Weber
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K160685 | 03/11/2016 | Surveyor S4 Mobile Monitor | Mortara Instrument, Inc. |
| K161517 | 06/02/2016 | Mortara Surveyor Patient Monitor | MORTARA INSTRUMENT, INC. |
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