FDA 510(k) Applications Submitted by Phamatech Inc.
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K070009 |
01/03/2007 |
AT HOME DRUG TEST MODELS, 9308T AND 9308X |
PHAMATECH INC. |
| K070098 |
01/10/2007 |
QUICKSCREEN BARBITURATE 300 SCREENING TEST, MODELS 9019, 9018; MULTI DRUG SCREENING TEST, MODEL 9317T; CUP MULTI DRUG SC |
PHAMATECH INC. |
| K040575 |
03/04/2004 |
PHARMATECH MENOPAUSE CHECK, MODELS 9111 AND 9112 |
PHAMATECH INC. |
| K013407 |
10/15/2001 |
AT HOME DRUG TEST, MODEL 9084 |
PHAMATECH INC. |
| K013408 |
10/15/2001 |
AT HOME DRUG TEST, MODEL 9079 |
PHAMATECH INC. |
| K013409 |
10/15/2001 |
AT HOME DRUG TEST, MODEL 9074 |
PHAMATECH INC. |
| K013410 |
10/15/2001 |
AT HOME DRUG TEST, MODEL 9064 |
PHAMATECH INC. |
| K013412 |
10/15/2001 |
AT HOME DRUG TEST, MODEL 9069 |
PHAMATECH INC. |
| K043051 |
11/04/2004 |
QUICKSCREEN OXYCODONE TEST, MODELS 9120, 9120T, 9120X AND 9121 |
PHAMATECH INC. |
| K103295 |
11/08/2010 |
QUICKSCREEN COCAINE 150 SCREENING TEST |
PHAMATECH INC. |
| K043167 |
11/16/2004 |
PHAMATECH QUICKSCREEN BENZODIAZEPINES TEST, MODELS 9025, 9026, 9027T, 9153T AND 9195X |
PHAMATECH INC. |
| K131069 |
04/17/2013 |
QUICKSCREEN AMPHETINE 500 TEST |
PHAMATECH INC. |
| K021409 |
05/03/2002 |
AT HOME OVULATION TEST, MODEL 9032 |
PHAMATECH INC. |
| K043599 |
12/29/2004 |
MOMENTS MENOPAUSE CHECK, MODEL 9113 |
PHAMATECH INC. |
| K181945 |
07/20/2018 |
QuickScreen Pro Multi Drug Screening Test, Model 9395Z |
Phamatech Inc. |
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