Ablative Solutions, Inc. is one of 16416 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Ablative Solutions, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Peregrine System Infusion Catheter 4-7 mm, Peregrine System Infusion Catheter 3-4 mm, PEREGRINE SYSTEM INFUSION CATHETER
2
Total
2
Cleared
0
Denied
Ablative Solutions, Inc. has 2 FDA 510(k) cleared medical devices. Based in Menlo Park, US.
Last cleared in 2023. Active since 2014. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Ablative Solutions, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Ablative Solutions, Inc.
2 devices