FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

AMEDITECH CHECKCUP MULTI DRUG TEST (FLAT/ROUND CUP)

K Number: K113501 · Decision Dec 5, 2011
Classifications
1
FEI Numbers
97
Registration Numbers
97
Same Product Code
144
Applicant Total
14
Review Days
10

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Basic Information

Device Name
AMEDITECH CHECKCUP MULTI DRUG TEST (FLAT/ROUND CUP)
K Number
K113501
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
862.3250
Medical Specialty
Clinical Toxicology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Ameditech, Inc.
Date Received
November 25, 2011
Decision Date
December 5, 2011
Product Code
DIO
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
DIO Enzyme Immunoassay, Cocaine And Cocaine Metabolites

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Other Clearances by Ameditech, Inc.

K Number Device Name
K113046 AMEDITECH IMMUTEST MILTI-DRUG SCREEN
K063015 AMEDITECH IMMUTEST MULTI-DRUG SCREEN BUP/PPX/COC150
K053175 AMEDITECH DRUGSMARTCUP
K050186 AMEDITECH IMMUTEST MULTI-DRUG SCREEN PANEL III
K042975 AMEDITECH IMMUTEST MULTI-DRUG SCREEN PANEL II
K040092 AMEDITECH IMMU TEST DRUG SCREEN PANEL
K023126 AMEDITECH IMMUTEST HCG PREGANCY TEST
K012483 AMEDITECH IMMUTEST DRUG SCREEN OPIATES
K012484 AMEDITECH IMMUTEST DRUG SCREEN AMPHETAMINE
K012582 AMEDITECH IMMUTEST DRUG SCREEN PCP
Search all 14 clearances from Ameditech, Inc. →