FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇦 Canada

ACETAMINOPHEN ASSAY

K Number: K952949 · Decision Sep 6, 1995
Classifications
1
FEI Numbers
21
Registration Numbers
21
Same Product Code
35
Applicant Total
66
Review Days
72

Basic Information

Device Name
ACETAMINOPHEN ASSAY
K Number
K952949
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.3030
Medical Specialty
Clinical Toxicology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
DIAGNOSTIC CHEMICALS LTD.
Date Received
June 26, 1995
Decision Date
September 6, 1995
Product Code
LDP
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
LDP Colorimetry, Acetaminophen

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