Bioptics, Inc. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Bioptics, Inc. has 4 FDA 510(k) cleared medical devices. Based in Tucson, US.
Historical record: 4 cleared submissions from 2005 to 2010. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Bioptics, Inc. Filter by specialty or product code using the sidebar.
4 devices
Cleared
Jun 16, 2010
10 X 10 VISION
Radiology
351d
Cleared
Jul 17, 2009
BIOVISION DIGITAL SPECIMEN RADIOGRAPHY SYSTEM
Radiology
50d
Cleared
Nov 21, 2008
CORE VISION DIGITAL SPECIMEN RADIOGRAPHY (DSR) SYSTEM
Radiology
91d
Cleared
Oct 18, 2005
PIXARRAY 100 DIGITAL SPECIMEN RADIOGRAPHY (DSR) SYSTEM
Radiology
42d