FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
AMEDITECH IMMUTEST MULTI-DRUG SCREEN PANEL III
K Number: K050186
·
Decision Mar 4, 2005
Classifications
1
FEI Numbers
96
Registration Numbers
96
Same Product Code
224
Applicant Total
14
Review Days
36
Research this 510(k) in seconds
The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.
Free to try · every answer cites its records
Basic Information
- Device Name
- AMEDITECH IMMUTEST MULTI-DRUG SCREEN PANEL III
- K Number
- K050186
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 862.3100
- Medical Specialty
- Clinical Toxicology
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- Ameditech, Inc.
- Date Received
- January 27, 2005
- Decision Date
- March 4, 2005
- Product Code
- DKZ
- Advisory Committee
- Clinical Toxicology
- Review Advisory Committee
- TX
- Third Party
- N
Classifications
This FDA 510(k) entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| DKZ | Enzyme Immunoassay, Amphetamine | FDA class 2 | Clinical Toxicology |
Similar 510(k) Clearances
Other 510(k) clearances with the same product code (DKZ), ordered by most recent decision date.
DRI Ecstasy Plus Assay
FDA 510(k)
FDA Class 2
·Clinical Toxicology
AllTest Multi-Drug Rapid Test Cup; AllTest Multi-Drug Rapid Test Panel; AllTest Multi-Drug Rapid Test Cup Rx; AllTest Multi-Drug Rapid Test Panel Rx
FDA 510(k)
FDA Class 2
·Clinical Toxicology
Xenta Drug Screen Cup, Xenta Drug Screen Dipcard
FDA 510(k)
FDA Class 2
·Clinical Toxicology
Quidel Triage® TOX Drug Screen, 94600
FDA 510(k)
FDA Class 2
·Clinical Toxicology
Atlas Multi-Drugs Screening Test Cup, Atlas Multi-Drugs Screening Test Panel
FDA 510(k)
FDA Class 2
·Clinical Toxicology
Quidel Triage TOX Drug Screen, 94600; Quidel Triage® MeterPro
FDA 510(k)
FDA Class 2
·Clinical Toxicology
Other Clearances by Ameditech, Inc.
| K Number | Device Name | ||
|---|---|---|---|
| K113501 | AMEDITECH CHECKCUP MULTI DRUG TEST (FLAT/ROUND CUP) | Dec 5, 2011 | Substantially Equivalent |
| K113046 | AMEDITECH IMMUTEST MILTI-DRUG SCREEN | Nov 10, 2011 | Substantially Equivalent |
| K063015 | AMEDITECH IMMUTEST MULTI-DRUG SCREEN BUP/PPX/COC150 | Dec 20, 2006 | Substantially Equivalent |
| K053175 | AMEDITECH DRUGSMARTCUP | Dec 8, 2005 | Substantially Equivalent |
| K042975 | AMEDITECH IMMUTEST MULTI-DRUG SCREEN PANEL II | Dec 29, 2004 | Substantially Equivalent |
| K040092 | AMEDITECH IMMU TEST DRUG SCREEN PANEL | Mar 8, 2004 | Substantially Equivalent |
| K023126 | AMEDITECH IMMUTEST HCG PREGANCY TEST | Nov 18, 2002 | Substantially Equivalent |
| K012483 | AMEDITECH IMMUTEST DRUG SCREEN OPIATES | Nov 30, 2001 | Substantially Equivalent |
| K012484 | AMEDITECH IMMUTEST DRUG SCREEN AMPHETAMINE | Nov 30, 2001 | Substantially Equivalent |
| K012582 | AMEDITECH IMMUTEST DRUG SCREEN PCP | Nov 30, 2001 | Substantially Equivalent |