Crossbay Medical is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Crossbay Medical - FDA 510(k) Cleared Devices
Recent clearances: CrossGlide ETS Plus, CrossBay Endometrial Tissue Sampler (ETS), CrossBay Cervical Dilator Catheter System
3
Total
3
Cleared
0
Denied
Crossbay Medical has 3 FDA 510(k) cleared medical devices. Based in San Diego, US.
Historical record: 3 cleared submissions from 2019 to 2020. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by Crossbay Medical Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Domecus Consulting Services, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Crossbay Medical
3 devices