FDA 510(k) Applications Submitted by Michael Wong

FDA 510(k) Number Submission Date Device Name Applicant
K222019 07/08/2022 Reprocessed RD SET Adt Pulse Oximeter Sensor (4000), Reprocessed RD SET Pdt Pulse Oximeter Sensor (4001), Reprocessed RD SET Inf Pulse Oximeter Sensor (4002), Reprocessed RD SET Adt Pulse Oximeter Sensor (4003) Stryker Sustainability Solutions
K243047 09/27/2024 Zoom 7X Catheter; Zoom Aspiration Tubing; Zoom POD Aspiration Tubing Imperative Care, Inc.


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