Germ Terminator Corporation is one of 25838 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Germ Terminator Corporation - FDA 510(k) Cleared Devices
Recent clearances: GERM TERMINATOR GT 100 TOOTHBRUSH SANITIZER
1
Total
1
Cleared
0
Denied
Germ Terminator Corporation has 1 FDA 510(k) cleared medical devices. Based in Concord, US.
Historical record: 1 cleared submissions from 2002 to 2002. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Germ Terminator Corporation Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Intertek Testing Services as regulatory consultant.
FDA 510(k) Regulatory Record - Germ Terminator Corporation
1 devices