Desert Harvest, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Desert Harvest, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Aloe Glide Lubricant
1
Total
1
Cleared
0
Denied
Desert Harvest, Inc. has 1 FDA 510(k) cleared medical devices. Based in Hillsborough, US.
Historical record: 1 cleared submissions from 2019 to 2019. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by Desert Harvest, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Amin Talati Wasserman, Llp as regulatory consultant.
FDA 510(k) Regulatory Record - Desert Harvest, Inc.
1 devices