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

ADVIA IMS CARBAMAZEPINE METHOD

K Number: K042808 · Decision Feb 8, 2005
Classifications
1
FEI Numbers
20
Registration Numbers
20
Same Product Code
55
Applicant Total
46
Review Days
119

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Basic Information

Device Name
ADVIA IMS CARBAMAZEPINE METHOD
K Number
K042808
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.3645
Medical Specialty
Clinical Toxicology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Bayer Healthcare, LLC
Date Received
October 12, 2004
Decision Date
February 8, 2005
Product Code
KLT
Advisory Committee
Clinical Toxicology
Review Advisory Committee
CH
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
KLT Enzyme Immunoassay, Carbamazepine

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K093930 DIDGET WORLD REPORTS
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K090413 A1CNOW+ (10 TEST KIT, PROFESSIONAL USE) MODEL 3024, A1CNOW+(20 TEST KIT, PROFESSIONAL USE) MODEL 3021, A1CNOW SELF CHEC
K082486 GLUCOFACTS EXPRESS DIABETES MANAGEMENT SOFTWARE
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