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
LCM Enzyme Immunoassay, Phencyclidine

Similar 510(k) Clearances

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

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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
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
Search all 14 clearances from Ameditech, Inc. →