Allergy Direct is one of 12164 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Allergy Direct - FDA 510(k) Cleared Devices
Recent clearances: EVENT ALLERGEN BARRIERS, EVENT MATTRESS ENCASING, EVENT DUVET ENCASING, EVENT PILLOW ENCASING, EVENT BEDDING SYSTEM
1
Total
1
Cleared
0
Denied
Allergy Direct has 1 FDA 510(k) cleared medical devices. Based in Kansas City, US.
Historical record: 1 cleared submissions from 1999 to 1999. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Allergy Direct Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Allergy Direct
1 devices