Dynarad Corp. - FDA 510(k) Cleared Devices
9
Total
9
Cleared
0
Denied
Dynarad Corp. has 9 FDA 510(k) cleared medical devices. Based in Deer Park, US.
Historical record: 9 cleared submissions from 1993 to 2000. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Dynarad Corp. Filter by specialty or product code using the sidebar.
9 devices
Cleared
Feb 10, 2000
X-RAY MONOBLOCK, MONOBLOCK XRS-60-330
Radiology
34d
Cleared
May 06, 1998
FACTS MONOBLOCK
Radiology
29d
Cleared
Dec 30, 1997
CONTROL, X-RAY DIAGNOSTIC, GENERATOR, HIGH VOLTAGE, ASSEMBLY, TUBE HOUSING...
Radiology
84d
Cleared
Feb 08, 1995
NOVA XM2
Radiology
636d
Cleared
Jul 20, 1994
PHANTOM
Radiology
121d
Cleared
Jan 31, 1994
HF-110A
Radiology
263d
Cleared
Aug 03, 1993
9150A, 1100F
Radiology
82d
Cleared
Jul 23, 1993
9170, 1170
Radiology
71d
Cleared
Jul 14, 1993
ALPHA II
Radiology
100d