FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

DUPONT ACA(R) URINE DRUGE OS ABUSE CONTROL

K Number: K952412 · Decision Jun 23, 1995
Classifications
1
FEI Numbers
41
Registration Numbers
41
Same Product Code
201
Applicant Total
28
Review Days
31

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Basic Information

Device Name
DUPONT ACA(R) URINE DRUGE OS ABUSE CONTROL
K Number
K952412
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.3280
Medical Specialty
Clinical Toxicology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Dupont Medical Products
Date Received
May 23, 1995
Decision Date
June 23, 1995
Product Code
DIF
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
DIF Drug Mixture Control Materials

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K944932 PHENOBARBITAL FLEX REAGENT CARTRIDGE
K941050 DUPONT ACA STAR
K943996 DUPONT ACA PLUS LUTEINIZING HORMONE (LH) METHOD
K941146 DUPONT ACA PLUS THYROID STIMULATING HORMONE SYSTEM
K942640 DUPONT DIMENSION AMYLASE METHOD
K942241 DUPONT APC BLOOD COLLECTION CONTAINER WITH THROMBOPLASTIN
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