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

TDX (R) AMPHETAMINE CLASS

K Number: K874770 · Decision Apr 21, 1988
Classifications
1
FEI Numbers
105
Registration Numbers
105
Same Product Code
223
Applicant Total
857
Review Days
154

Basic Information

Device Name
TDX (R) AMPHETAMINE CLASS
K Number
K874770
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.3100
Medical Specialty
Clinical Toxicology
Decision
Substantially Equivalent
Applicant
ABBOTT LABORATORIES
Date Received
November 19, 1987
Decision Date
April 21, 1988
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

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