Alphatek Corp. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Alphatek Corp. has 5 FDA 510(k) cleared medical devices. Based in Chicago, US.
Historical record: 5 cleared submissions from 1992 to 2003. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Alphatek Corp. Filter by specialty or product code using the sidebar.
5 devices
Cleared
Jan 23, 2003
AX200 AUTOMATIC X-RAY FILM PROCESSOR, MODEL 6586.036
Radiology
87d
Cleared
Aug 23, 1993
MAMMO-300 AUTOMATIC X-RAY FILM PROCESSOR
Radiology
131d
Cleared
Aug 23, 1993
AX-390SE AUTOMATIC X-RAY FILM PROCESSOR 9586.033
Radiology
131d
Cleared
Jan 15, 1993
AX-700LE AUTOMATIC X-RAY FILM PROCESSOR
Radiology
73d
Cleared
Nov 27, 1992
AX-300SE AUTOMATIC X-RAY FILM PROCESSOR, 6586.027
Radiology
87d