FDA 510(k) Applications Submitted by Elliquence, LLC
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K180766 | 03/23/2018 | Endiscope, Endiscope Cervical | Elliquence, LLC |
| K170107 | 01/12/2017 | Surgi Max Ultra | elliquence, LLC |
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