Mays and Associates, Inc. is one of 25397 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Mays and Associates, Inc. - FDA 510(k) Cleared Devices
Recent clearances: OMNIPRO SYSTEM
1
Total
1
Cleared
0
Denied
Mays and Associates, Inc. has 1 FDA 510(k) cleared medical devices. Based in Houston, US.
Historical record: 1 cleared submissions from 2005 to 2005. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Mays and Associates, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Entela, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Mays and Associates, Inc.
1 devices