Carrashield Labs, Inc. is one of 18443 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Carrashield Labs, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Divine 9
1
Total
1
Cleared
0
Denied
Carrashield Labs, Inc. has 1 FDA 510(k) cleared medical devices. Based in Orlando, US.
Historical record: 1 cleared submissions from 2015 to 2015. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by Carrashield Labs, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by O'Connell Regulatory Consultants, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Carrashield Labs, Inc.
1 devices