Phamatech is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Phamatech - FDA 510(k) Cleared Devices
Recent clearances: QUICKSCREEN, MODELS 9177X AND 9178X, AT HOME DRUG CUP, MODEL 9150X, AT WORK DRUG TEST, MODEL 9177T AWT
47
Total
47
Cleared
0
Denied
Phamatech has 47 FDA 510(k) cleared toxicology devices. Based in San Diego, US.
Historical record: 47 cleared submissions from 1996 to 2004.
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 - Phamatech
47 devices
Cleared
Sep 10, 2004
QUICKSCREEN, MODELS 9177X AND 9178X
Chemistry
88d
Cleared
Apr 14, 2003
AT HOME DRUG CUP, MODEL 9150X
Toxicology
62d
Cleared
Apr 11, 2001
AT WORK DRUG TEST, MODEL 9177T AWT
Toxicology
22d
Cleared
Apr 11, 2001
AT WORK DRUG TEST, MODEL 9147T AWT
Toxicology
22d
Cleared
Apr 05, 2001
AT HOME DRUG TEST, MODEL 9068 T
Toxicology
31d
Cleared
Apr 05, 2001
AT HOME DRUG TEST, MODEL 9078 T
Toxicology
31d
Cleared
Apr 05, 2001
AT HOME DRUG TESTT, MODEL 9150 T
Toxicology
31d
Cleared
Mar 30, 2001
AT HOME DRUG TEST, MODEL 9063 T
Toxicology
25d
Cleared
Mar 30, 2001
AT HOME DRUG TEST, MODEL 9083 T
Toxicology
25d
Cleared
Mar 30, 2001
AT HOME DRUG TEST, MODEL 9073 T
Toxicology
25d
Cleared
Mar 30, 2001
AT HOME DRUG TEST, MODEL 9133 T
Toxicology
25d
Cleared
Feb 12, 2001
MODIFICATION TO AT HOME DRUG TEST, MODELS 9150, 9068, AND 9175
Toxicology
61d
Looking for a specific device from Phamatech? Search by device name or K-number.
Search all Phamatech devices