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

AMEDITECH IMMU TEST DRUG SCREEN PANEL

K Number: K040092 · Decision Mar 8, 2004
Classifications
1
FEI Numbers
96
Registration Numbers
96
Same Product Code
224
Applicant Total
14
Review Days
52

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 IMMU TEST DRUG SCREEN PANEL
K Number
K040092
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
862.3100
Medical Specialty
Clinical Toxicology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Ameditech, Inc.
Date Received
January 16, 2004
Decision Date
March 8, 2004
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
DKZ Enzyme Immunoassay, Amphetamine

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (DKZ), ordered by most recent decision date.

View all

Other Clearances by Ameditech, Inc.

K Number Device Name
K113501 AMEDITECH CHECKCUP MULTI DRUG TEST (FLAT/ROUND CUP)
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
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. →