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

QUEST DIAGNOSTICS HAIRCHECK-DT (THC)

K Number: K040257 · Decision Jun 14, 2004
Classifications
1
FEI Numbers
103
Registration Numbers
103
Same Product Code
149
Applicant Total
7
Review Days
131

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
QUEST DIAGNOSTICS HAIRCHECK-DT (THC)
K Number
K040257
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.3870
Medical Specialty
Clinical Toxicology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Quest Diagnostics, Inc.
Date Received
February 4, 2004
Decision Date
June 14, 2004
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

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (LDJ), ordered by most recent decision date.

View all

Other Clearances by Quest Diagnostics, Inc.

K Number Device Name
K080381 QUEST DIAGNOSTICS METHAMPHETAMINE MICRO-PLATE EIA
K062929 QUEST DIAGNOSTICS URINE COCAINE METABOLITE EIA
K051161 QUEST DIAGNOSTICS HAIRCHECK-DT (AMPHETAMINES)
K042726 QUEST DIAGNOSTICS HAIRCHECK-DT (PCP
K042725 QUEST DIAGNOSTICS HAIRCHECK-DT (OPIATES)
K023626 AML HAIRCHECK-DT (COCAINE)