Alara, Inc. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Alara, Inc. has 6 FDA 510(k) cleared medical devices. Based in Hayward, US.
Historical record: 6 cleared submissions from 2000 to 2011. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Alara, Inc. Filter by specialty or product code using the sidebar.
6 devices
Cleared
Jun 02, 2011
ALARA T210 COMPUTED RADIOGRAPHY SYSTEM
Radiology
276d
Cleared
Aug 15, 2007
CRYSTALVIEW T-SERIES COMPUTED RADIOGRAPHY SYSTEM, MODELS T110 (WITH ERASER)...
Radiology
57d
Cleared
Sep 18, 2006
CRYSTALVIEW R200
Radiology
33d
Cleared
Jun 30, 2006
ALARA CRYSTALVIEW COMPUTED RADIOGRAPHY SYSTEM, MODEL R200
Radiology
28d
Cleared
Oct 02, 2003
ALARA CRYSTALVIEW COMPUTED RADIOGRAPHY SYSTEM
Radiology
73d
Cleared
May 12, 2000
METRISCAN BONE DENSITY SYSTEM
Radiology
114d