Proteus Digital Health, Inc. is one of 5098 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Proteus Digital Health, Inc. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Proteus Digital Health, Inc. has 4 FDA 510(k) cleared medical devices. Based in Redwood City, US.
Historical record: 4 cleared submissions from 2013 to 2015. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Proteus Digital Health, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Proteus Digital Health, Inc.
4 devices
Cleared
Jun 27, 2015
Proteus Digital Health Feedback Device
Gastroenterology & Urology
122d
Cleared
Feb 07, 2014
PROTEUS PATCH, PROTEUS INGESTIBLE SENSOR (ACCESSORY)
Gastroenterology & Urology
107d
Cleared
Jun 23, 2013
PROTEUS PATCH INCLUDING INGESTIBLE SENSOR
Gastroenterology & Urology
26d
Cleared
May 07, 2013
PROTEUS PATCH, INGESTIBLE SENSOR (ACCESSORY)
Gastroenterology & Urology
26d