Medical Device Manufacturer · US , Prescott , AZ

Persyst Development Corp. - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 1998

Total

Cleared

Denied

Persyst Development Corp. has 4 FDA 510(k) cleared medical devices. Based in Prescott, US.

Historical record: 4 cleared submissions from 1998 to 2013. Primary specialty: Neurology.

Browse the FDA 510(k) cleared devices submitted by Persyst Development Corp. Filter by specialty or product code using the sidebar.

Persyst Development Corp. is one of 5153 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

Persyst Development Corp. — FDA 510(k) Products and Clearance History

4 devices

1-4 of 4