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

DBEST TETRAHYDROCANNABINOL TEST KIT

K Number: K983188 · Decision Nov 18, 1998
Classifications
1
FEI Numbers
103
Registration Numbers
103
Same Product Code
149
Applicant Total
17
Review Days
68

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Basic Information

Device Name
DBEST TETRAHYDROCANNABINOL TEST KIT
K Number
K983188
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.3870
Medical Specialty
Clinical Toxicology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Ameritek, Inc.
Date Received
September 11, 1998
Decision Date
November 18, 1998
Product Code
LDJ
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
LDJ Enzyme Immunoassay, Cannabinoids

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K984269 DBEST OCCULT BLOOD TEST KIT
K983191 DBEST COCAINE TEST KIT
K983190 DBEST OPIATES TEST KIT
K983189 DBEST METHAMPHETAMINES TEST KIT
K981504 DBEST AMPHETAMINES TEST KIT
K974508 DBEST ONE-STEP OVULATION TEST
K973957 DBEST ONE-STEP HCG SERUM/URINE TEST
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