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

HYCOR ACCUPINCH COCAINE TEST

K Number: K896937 · Decision Mar 6, 1990
Classifications
1
FEI Numbers
97
Registration Numbers
97
Same Product Code
144
Applicant Total
51
Review Days
83

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Basic Information

Device Name
HYCOR ACCUPINCH COCAINE TEST
K Number
K896937
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.3250
Medical Specialty
Clinical Toxicology
Decision
Substantially Equivalent
Applicant
Hycor Biomedical, Inc.
Date Received
December 13, 1989
Decision Date
March 6, 1990
Product Code
DIO
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
DIO Enzyme Immunoassay, Cocaine And Cocaine Metabolites

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Other Clearances by Hycor Biomedical, Inc.

K Number Device Name
K081217 HY-TEC SPECIFIC AND TOTAL IGE EIA SYSTEM
K080322 HY*TEC EXTENDED SPECIFIC IGE EIA, MCS ASSAY USING TECAN FREEDOM EVO RSP 200
K022944 AUTOSTAT II ANTI-B-2 GLYCOPROTEIN-I IGM ELISA
K022945 AUTOSTAT II ANTI-B-2 GLYCOPROTEIN I IGG ELISA
K965094 HYCOR ALLERGEN DISC
K962730 HYCOR HY.TEC/MANUAL DS-DNA AUTO-ANTIBODY
K962720 HYCOR HY.TEC/MANUAL SCL-70 AUTO-ANTIBODY
K962729 HYCOR HY.TEC/MANUAL RF AUTO-ANTIBODY
K962578 HYCOR HY.TEC/MANUAL SS-B AUTO-ANTIBODY
K962722 HYCOR HY.TEC/MANUAL SM AUTO-ANTIBODY
Search all 51 clearances from Hycor Biomedical, Inc. →