Phamatech, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Phamatech, Inc. - FDA 510(k) Cleared Devices
Recent clearances: QuickScreen Pro Multi Drug Screening Test, Model 9395Z
15
Total
15
Cleared
0
Denied
Phamatech, Inc. has 15 FDA 510(k) cleared medical devices. Based in San Diego, US.
Historical record: 15 cleared submissions from 2001 to 2018. Primary specialty: Toxicology.
Browse the FDA 510(k) cleared devices submitted by Phamatech, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by KARA & Associates as regulatory consultant.
FDA 510(k) Regulatory Record - Phamatech, Inc.
15 devices
Cleared
Oct 18, 2018
QuickScreen Pro Multi Drug Screening Test, Model 9395Z
Toxicology
90d
Cleared
May 14, 2014
QUICKSCREEN AMPHETINE 500 TEST
Toxicology
392d
Cleared
Feb 01, 2012
QUICKSCREEN COCAINE 150 SCREENING TEST
Toxicology
450d
Cleared
Dec 07, 2007
AT HOME DRUG TEST MODELS, 9308T AND 9308X
Toxicology
338d
Cleared
Dec 07, 2007
QUICKSCREEN BARBITURATE 300 SCREENING TEST, MODELS 9019, 9018
Toxicology
331d
Cleared
Feb 25, 2005
MOMENTS MENOPAUSE CHECK, MODEL 9113
Chemistry
58d
Cleared
Feb 07, 2005
QUICKSCREEN OXYCODONE TEST, MODELS 9120, 9120T, 9120X AND 9121
Chemistry
95d
Cleared
Dec 29, 2004
PHAMATECH QUICKSCREEN BENZODIAZEPINES TEST, MODELS 9025, 9026, 9027T, 9153T...
Chemistry
43d
Cleared
May 20, 2004
PHARMATECH MENOPAUSE CHECK, MODELS 9111 AND 9112
Chemistry
77d
Cleared
May 24, 2002
AT HOME OVULATION TEST, MODEL 9032
Chemistry
21d
Cleared
Dec 06, 2001
AT HOME DRUG TEST, MODEL 9084
Toxicology
52d
Cleared
Dec 06, 2001
AT HOME DRUG TEST, MODEL 9079
Toxicology
52d
Cleared
Dec 06, 2001
AT HOME DRUG TEST, MODEL 9074
Toxicology
52d
Cleared
Dec 06, 2001
AT HOME DRUG TEST, MODEL 9064
Toxicology
52d
Cleared
Dec 06, 2001
AT HOME DRUG TEST, MODEL 9069
Toxicology
52d