QuickScreen Pro Multi Drug Screening Test, Model 9395Z— 510(k) K181945
Substantially EquivalentPhamatech, Inc.
FDA 510(k) clearance K181945 for QuickScreen Pro Multi Drug Screening Test, Model 9395Z, Substantially Equivalent on 2018-10-18. Applicant: Phamatech, Inc.. Device class: 2.
Clearance details
- Applicant
- Phamatech, Inc.
- Product code
- Code DKZ
- Device class
- Class 2
- Regulation
- 21 CFR 862.3100
- Advisory panel
- Clinical Toxicology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- San Diego, CA, US
Recent devices under product code DKZ
view allMore clearances from Phamatech, Inc.
view all- 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
Data sourced from openFDA. This site is unofficial and independent of the FDA.