Phamatech, Inc.
FDA 510(k) & PMA Approved Devices — 14 products
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Total Devices14
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K181945 | QuickScreen Pro Multi Drug Screening Test, Model 9395Z | DKZ | 2018-10-18 | View |
| 510(k) | K103295 | QUICKSCREEN COCAINE 150 SCREENING TEST | DIO | 2012-02-01 | View |
| 510(k) | K070009 | AT HOME DRUG TEST MODELS, 9308T AND 9308X | DIS | 2007-12-07 | View |
| 510(k) | K070098 | QUICKSCREEN BARBITURATE 300 SCREENING TEST, MODELS 9019, 9018; MULTI DRUG SCREENING TEST, MODEL 9317T; CUP MULTI DRUG SC | DIS | 2007-12-07 | View |
| 510(k) | K043599 | MOMENTS MENOPAUSE CHECK, MODEL 9113 | CGJ | 2005-02-25 | View |
| 510(k) | K043051 | QUICKSCREEN OXYCODONE TEST, MODELS 9120, 9120T, 9120X AND 9121 | DJG | 2005-02-07 | View |
| 510(k) | K043167 | PHAMATECH QUICKSCREEN BENZODIAZEPINES TEST, MODELS 9025, 9026, 9027T, 9153T AND 9195X | JXM | 2004-12-29 | View |
| 510(k) | K040575 | PHARMATECH MENOPAUSE CHECK, MODELS 9111 AND 9112 | CGJ | 2004-05-20 | View |
| 510(k) | K021409 | AT HOME OVULATION TEST, MODEL 9032 | CEP | 2002-05-24 | View |
| 510(k) | K013410 | AT HOME DRUG TEST, MODEL 9064 | MVO | 2001-12-06 | View |
| 510(k) | K013412 | AT HOME DRUG TEST, MODEL 9069 | MVO | 2001-12-06 | View |
| 510(k) | K013407 | AT HOME DRUG TEST, MODEL 9084 | DJG | 2001-12-06 | View |
| 510(k) | K013409 | AT HOME DRUG TEST, MODEL 9074 | MVO | 2001-12-06 | View |
| 510(k) | K013408 | AT HOME DRUG TEST, MODEL 9079 | DJG | 2001-12-06 | View |
No matching devices.
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