Dgh Technology, Inc. - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Dgh Technology, Inc. has 7 FDA 510(k) cleared medical devices. Based in Frazer, US.
Historical record: 7 cleared submissions from 1987 to 2017. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Dgh Technology, Inc. Filter by specialty or product code using the sidebar.
7 devices
Cleared
Jul 31, 2017
Scanmate Flex
Radiology
89d
Cleared
Apr 05, 2010
MODEL DGH 6000 SCANMATE A
Radiology
158d
Cleared
Nov 07, 2003
DGH 55 HANDHELD PACHYMETER (PACHMATE)
Radiology
15d
Cleared
Mar 17, 1997
DGH MODEL 9000
Ophthalmic
84d
Cleared
Nov 02, 1992
DGH-500 PACHYMETER
Radiology
249d
Cleared
Jan 31, 1992
DGH-4000 A-SCAN/PACHYMETER
Radiology
204d
Cleared
Dec 04, 1987
DGH-3000A A-SCAN
Radiology
149d