Kretztechnik AG - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Kretztechnik AG has 6 FDA 510(k) cleared medical devices. Based in Solon, US.
Historical record: 6 cleared submissions from 1990 to 1993. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Kretztechnik AG Filter by specialty or product code using the sidebar.
6 devices
Cleared
Jul 08, 1993
COMBISON(R) 311
Radiology
259d
Cleared
Oct 09, 1992
COMBISON(R) 330, MODEL # IR17.5AG/A & VRW177AK/A
Radiology
766d
Cleared
Apr 17, 1992
SECTOR TRANSDUCER MODEL NO. AWP3.5/A
Radiology
408d
Cleared
Jan 11, 1991
MODEL IW17.5A INTRA OPERATIVE TRANSDUCER
Radiology
88d
Cleared
Aug 15, 1990
ADD'L TRANSDUCER FOR USE W/THE COMBISON 310A
Radiology
121d
Cleared
Jul 20, 1990
1 TRANSDUCER FOR COMBISON 310A
Radiology
102d