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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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