FDA 510(k) Applications Submitted by Brenda Geary
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K150169 | 01/26/2015 | Sertera Biopsy Device | Hologic, INC |
| K191685 | 06/24/2019 | PicoWay Laser System | Candela Corporation |
| K180233 | 01/29/2018 | Eviva Stereotactic Guided Breast Biopsy System | Hologic, Inc |
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