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

VERDICT-II PROPOXYPHENE

K Number: K020787 · Decision May 2, 2002
Classifications
1
FEI Numbers
56
Registration Numbers
56
Same Product Code
21
Applicant Total
21
Review Days
52

Basic Information

Device Name
VERDICT-II PROPOXYPHENE
K Number
K020787
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.3700
Medical Specialty
Clinical Toxicology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
MEDTOX DIAGNOSTICS, INC.
Date Received
March 11, 2002
Decision Date
May 2, 2002
Product Code
JXN
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
JXN Enzyme Immunoassay, Propoxyphene

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K Number Device Name
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K091454 PROFILE-V MEDTOXSCAN DRUGS OF ABUSE TEST SYSTEM
K080635 MEDTOXSCAN
K060351 MEDTOX OXYCODONE
K050394 SURE-SCREEN AMPHETAMINE, BENZODIAZEPINE, COCAINE, METHAMPHETAMINE/MDMA, METHADONE, OPIATES, PHENCYCLIDINE & CANNABINOIDS
K033334 PROFILE -ER
K031032 VERDICT II, PROFILE II
K022141 VERDICT-II
K011545 VERDICT -II TCA, VERDICT-II MTD
Search all 21 clearances from MEDTOX DIAGNOSTICS, INC. →