Mediphysics Pain Centers of America is one of 25779 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Mediphysics Pain Centers of America - FDA 510(k) Cleared Devices
Recent clearances: MEDIPHYSICS PAIN TREATMENT SYSTEM, MODEL 1
1
Total
1
Cleared
0
Denied
Mediphysics Pain Centers of America has 1 FDA 510(k) cleared medical devices. Based in Lake Forest, US.
Historical record: 1 cleared submissions from 2003 to 2003. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Mediphysics Pain Centers of America Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Underwriters Laboratories, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Mediphysics Pain Centers of America
1 devices