FDA 510(k)
FDA unclassified
Substantially Equivalent
🇺🇸 United States
AMEDITECH IMMUTEST DRUG SCREEN PCP
K Number: K012582
·
Decision Nov 30, 2001
Classifications
1
FEI Numbers
96
Registration Numbers
96
Same Product Code
87
Applicant Total
14
Review Days
112
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Basic Information
- Device Name
- AMEDITECH IMMUTEST DRUG SCREEN PCP
- K Number
- K012582
- Device Class
- FDA unclassified
- Clearance Type
- Traditional
- Medical Specialty
- Unknown
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- Ameditech, Inc.
- Date Received
- August 10, 2001
- Decision Date
- November 30, 2001
- Product Code
- LCM
- Advisory Committee
- Unknown
- 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 |
|---|---|---|---|
| LCM | Enzyme Immunoassay, Phencyclidine | FDA unclassified | Unknown |
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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 |
| K050186 | AMEDITECH IMMUTEST MULTI-DRUG SCREEN PANEL III | Mar 4, 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 |