Phamatech, Inc.
Phamatech, Inc. holds FDA 510(k) medical device clearances, first cleared 2001, most recent 2018.
Top product codes for Phamatech, Inc.
Recent clearances by Phamatech, Inc.
- K181945 — QuickScreen Pro Multi Drug Screening Test, Model 9395Z
- K131069 — QUICKSCREEN AMPHETINE 500 TEST
- K103295 — QUICKSCREEN COCAINE 150 SCREENING TEST
- K070009 — AT HOME DRUG TEST MODELS, 9308T AND 9308X
- K070098 — QUICKSCREEN BARBITURATE 300 SCREENING TEST, MODELS 9019, 9018; MULTI DRUG SCREENING TEST, MODEL 9317T; CUP MULTI DRUG SC
- K043599 — MOMENTS MENOPAUSE CHECK, MODEL 9113
- K043051 — QUICKSCREEN OXYCODONE TEST, MODELS 9120, 9120T, 9120X AND 9121
- K043167 — PHAMATECH QUICKSCREEN BENZODIAZEPINES TEST, MODELS 9025, 9026, 9027T, 9153T AND 9195X
- K040575 — PHARMATECH MENOPAUSE CHECK, MODELS 9111 AND 9112
- K021409 — AT HOME OVULATION TEST, MODEL 9032
- K013407 — AT HOME DRUG TEST, MODEL 9084
- K013408 — AT HOME DRUG TEST, MODEL 9079
- K013409 — AT HOME DRUG TEST, MODEL 9074
- K013410 — AT HOME DRUG TEST, MODEL 9064
- K013412 — AT HOME DRUG TEST, MODEL 9069
Data sourced from openFDA. This site is unofficial and independent of the FDA.