Carrot, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Carrot, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Pivot Breath Sensor
1
Total
1
Cleared
0
Denied
Carrot, Inc. has 1 FDA 510(k) cleared medical devices. Based in Redwood City, US.
Last cleared in 2021. Active since 2021. Primary specialty: Toxicology.
Browse the FDA 510(k) cleared devices submitted by Carrot, 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, Inc.
1 devices