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

DBEST AMPHETAMINES TEST KIT

K Number: K981504 · Decision Aug 6, 1998
Classifications
1
FEI Numbers
96
Registration Numbers
96
Same Product Code
224
Applicant Total
17
Review Days
101

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Basic Information

Device Name
DBEST AMPHETAMINES TEST KIT
K Number
K981504
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.3100
Medical Specialty
Clinical Toxicology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Ameritek, Inc.
Date Received
April 27, 1998
Decision Date
August 6, 1998
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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Other Clearances by Ameritek, Inc.

K Number Device Name
K001215 DBEST HCG 2 IU/ML TEST KIT
K990873 DBEST URINARY TRACT INFECTION TEST KIT FOR HOME-USE
K990681 DBSET MULTIDRUG SCREEN TEST KIT
K984269 DBEST OCCULT BLOOD TEST KIT
K983191 DBEST COCAINE TEST KIT
K983188 DBEST TETRAHYDROCANNABINOL TEST KIT
K983190 DBEST OPIATES TEST KIT
K983189 DBEST METHAMPHETAMINES TEST KIT
K974508 DBEST ONE-STEP OVULATION TEST
K973957 DBEST ONE-STEP HCG SERUM/URINE TEST
Search all 17 clearances from Ameritek, Inc. →