Harbour Health, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Harbour Health, LLC - FDA 510(k) Cleared Devices
Recent clearances: Powder Free Nitrile Examination Glove, Tested for Use with Chemoterapy Drugs (Blue)
1
Total
1
Cleared
0
Denied
Harbour Health, LLC has 1 FDA 510(k) cleared medical devices. Based in Newport Beach, US.
Last cleared in 2021. Active since 2021. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Harbour Health, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Third Party Review Group, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Harbour Health, LLC
1 devices