Therapeutics 101, Inc (Dba Pressure Point, Inc.) is one of 23224 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Therapeutics 101, Inc (Dba Pressure Point, Inc.) - FDA 510(k) Cleared...
Recent clearances: PRESSURE RIGHT, SINGLE-USE, DISPOSABLE, PRESSURE-SENSITIVE EMETIC-MANAGEMENT WRIST STRIP
1
Total
1
Cleared
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Denied
Therapeutics 101, Inc (Dba Pressure Point, Inc.) has 1 FDA 510(k) cleared medical devices. Based in Austin, US.
Historical record: 1 cleared submissions from 2011 to 2011. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Therapeutics 101, Inc (Dba Pressure Point, Inc.) Filter by specialty or product code using the sidebar.
1 device has linked clinical trial registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Therapeutics 101, Inc (Dba Pressure Point, Inc.)
1 devices