Dyna Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Dyna Corp. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Dyna Corp. has 5 FDA 510(k) cleared medical devices. Based in Carlsbad, US.
Historical record: 5 cleared submissions from 1990 to 1997. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Dyna Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Dyna Corp.
5 devices
Cleared
Jul 28, 1997
DYNA GLIDE 2600 ROLL-IN AMBULANCE COT (95759)
General Hospital
21d
Cleared
Aug 01, 1996
HARE MODEL 2000 EZ LOADER MODEL 95555
General Hospital
56d
Cleared
Jun 26, 1990
HARE FOLDING BACK EMERGENCY STRETCHER
General Hospital
21d
Cleared
Apr 23, 1990
HARE EMERGENCY STRETCHER
General Hospital
69d
Cleared
Apr 23, 1990
HARE EMERGENCY STRETCHER WITH WHEELS
General Hospital
69d