Howtek, Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Howtek, Inc. has 5 FDA 510(k) cleared medical devices. Based in Hudson, US.
Historical record: 5 cleared submissions from 1996 to 2002. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Howtek, Inc. Filter by specialty or product code using the sidebar.
5 devices
Cleared
Aug 12, 2002
FULCRUM
Radiology
60d
Cleared
Nov 05, 1997
DIGITIZER DIRECTOR: IMAGE COMPRESSION MODULE (HO4059-REV 2.0)
Radiology
79d
Cleared
Sep 08, 1997
DIGITIZER DIRECTOR (HSC025-01)
Radiology
90d
Cleared
May 20, 1997
HOWTEK 960
Radiology
70d
Cleared
Jan 18, 1996
SCANMASTER DX
Radiology
199d