Perma Laboratories is one of 24558 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
1
Total
1
Cleared
0
Denied
Perma Laboratories has 1 FDA 510(k) cleared medical devices. Based in Hinckley, US.
Historical record: 1 cleared submissions from 2012 to 2012. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Perma Laboratories Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Perma Laboratories
1 devices