Perimeter Medical Imaging Ai, Inc. is one of 208 FDA 510(k) medical device manufacturers from Canada in the dataset, ranked by real submission volume.
Perimeter Medical Imaging Ai, Inc. - FDA 510(k) Cleared Devices
Recent clearances: OTIS 2.1 Optical Coherence Tomography System, THiA Optical Coherence Tomography System
1
Total
1
Cleared
0
Denied
Perimeter Medical Imaging Ai, Inc. has 1 FDA 510(k) cleared medical devices. Based in Toronto, CA.
Last cleared in 2021. Active since 2021. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Perimeter Medical Imaging Ai, Inc. 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 - Perimeter Medical Imaging Ai, Inc.
1 devices