Ameditech, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Ameditech, Inc. - FDA 510(k) Cleared Devices
14
Total
14
Cleared
0
Denied
Ameditech, Inc. has 14 FDA 510(k) cleared toxicology devices. Based in San Diego, US.
Historical record: 14 cleared submissions from 2001 to 2011.
Browse the complete list of FDA 510(k) cleared toxicology devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Ameditech, Inc.
14 devices
Cleared
Dec 05, 2011
AMEDITECH CHECKCUP MULTI DRUG TEST (FLAT/ROUND CUP)
Toxicology
10d
Cleared
Nov 10, 2011
AMEDITECH IMMUTEST MILTI-DRUG SCREEN
Toxicology
28d
Cleared
Dec 20, 2006
AMEDITECH IMMUTEST MULTI-DRUG SCREEN BUP/PPX/COC150
Toxicology
79d
Cleared
Dec 08, 2005
AMEDITECH DRUGSMARTCUP
Toxicology
24d
Cleared
Mar 04, 2005
AMEDITECH IMMUTEST MULTI-DRUG SCREEN PANEL III
Toxicology
36d
Cleared
Dec 29, 2004
AMEDITECH IMMUTEST MULTI-DRUG SCREEN PANEL II
Toxicology
62d
Cleared
Mar 08, 2004
AMEDITECH IMMU TEST DRUG SCREEN PANEL
Toxicology
52d
Cleared
Nov 18, 2002
AMEDITECH IMMUTEST HCG PREGANCY TEST
Chemistry
60d
Cleared
Nov 30, 2001
AMEDITECH IMMUTEST DRUG SCREEN OPIATES
Toxicology
120d
Cleared
Nov 30, 2001
AMEDITECH IMMUTEST DRUG SCREEN AMPHETAMINE
Toxicology
120d
Cleared
Nov 30, 2001
AMEDITECH IMMUTEST DRUG SCREEN PCP
Toxicology
112d
Cleared
Nov 16, 2001
AMEDITECH IMMUTEST DRUG SCREEN METHAMPHETAMINE
Toxicology
98d