QUICKSCREEN OXYCODONE TEST, MODELS 9120, 9120T, 9120X AND 9121— 510(k) K043051
Substantially EquivalentPhamatech, Inc.
FDA 510(k) clearance K043051 for QUICKSCREEN OXYCODONE TEST, MODELS 9120, 9120T, 9120X AND 9121, Substantially Equivalent on 2005-02-07. Applicant: Phamatech, Inc.. Device class: 2.
Clearance details
- Applicant
- Phamatech, Inc.
- Product code
- Code DJG
- Device class
- Class 2
- Regulation
- 21 CFR 862.3650
- Advisory panel
- Clinical Toxicology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- San Diego, CA, US
Recent devices under product code DJG
view allMore clearances from Phamatech, Inc.
view all- 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
Data sourced from openFDA. This site is unofficial and independent of the FDA.