Pressure Point, Inc. is one of 23208 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Pressure Point, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Pressure Right, Single-Use, Disposable, Acupressure, Pressure-Sensitive Wrist Strip
1
Total
1
Cleared
0
Denied
Pressure Point, Inc. has 1 FDA 510(k) cleared medical devices. Based in Tinton Falls, US.
Historical record: 1 cleared submissions from 2014 to 2014. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Pressure Point, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Emergo Group as regulatory consultant.
FDA 510(k) Regulatory Record - Pressure Point, Inc.
1 devices