Carrot Sense, Inc. is one of 14023 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Carrot Sense, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Carbon Monoxide Breath Sensor System (COBSS)
1
Total
1
Cleared
0
Denied
Carrot Sense, Inc. has 1 FDA 510(k) cleared medical devices. Based in Redwood City, US.
Historical record: 1 cleared submissions from 2017 to 2017. Primary specialty: Toxicology.
Browse the FDA 510(k) cleared devices submitted by Carrot Sense, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Hogan Lovells US LLP as regulatory consultant. 1 device has linked clinical trial registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Carrot Sense, Inc.
1 devices