Sanitas, Inc. is one of 16417 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Sanitas, Inc. - FDA 510(k) Cleared Devices
Recent clearances: FAMILY HEALTHWARE, WELLAHO PERSONALIZED OUTPATIENT MANAGEMENT SYSTEM
2
Total
2
Cleared
0
Denied
Sanitas, Inc. has 2 FDA 510(k) cleared medical devices. Based in San Diego, US.
Historical record: 2 cleared submissions from 2013 to 2014. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Sanitas, 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 - Sanitas, Inc.
2 devices