FDA 510(k) Applications Submitted by CooperSurgical Inc.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K191020 | 04/17/2019 | G210 InviCell Plus with SignipHy pH monitoring | CooperSurgical Inc. |
| K182959 | 10/25/2018 | Wallace Dual Lumen Oocyte Recovery System | CooperSurgical Inc. |
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