Synapse Electroceutical Limited is one of 490 FDA 510(k) medical device manufacturers from United Kingdom in the dataset, ranked by real submission volume.
Synapse Electroceutical Limited - FDA 510(k) Cleared Devices
Recent clearances: Synapse Transcutaneous Electrical Stimulation Device
1
Total
1
Cleared
0
Denied
Synapse Electroceutical Limited has 1 FDA 510(k) cleared medical devices. Based in Westerham, GB.
Historical record: 1 cleared submissions from 2015 to 2015. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Synapse Electroceutical Limited Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Martin,Blank & Associates as regulatory consultant.
FDA 510(k) Regulatory Record - Synapse Electroceutical Limited
1 devices