FDA 510(k) FDA class 1 Substantially Equivalent 🇨🇦 Canada

CHOLINESTERASE ASSAY KIT, CATALOGUE# 300-05

K Number: K955498 · Decision Jan 24, 1996
Classifications
1
FEI Numbers
23
Registration Numbers
23
Same Product Code
25
Applicant Total
66
Review Days
54

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Basic Information

Device Name
CHOLINESTERASE ASSAY KIT, CATALOGUE# 300-05
K Number
K955498
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.3240
Medical Specialty
Clinical Toxicology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Diagnostic Chemicals , Ltd.
Date Received
December 1, 1995
Decision Date
January 24, 1996
Product Code
DIH
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
DIH Colorimetry, Cholinesterase

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K060139 CRP-ADVANCE ASSAY, MODELS 250-20, 250-25
K060140 CRP-ADVANCE MULTI CALIBRATOR SET, MODEL SE-250
K051757 CALCIUM ADVANCE ASSAY, MODEL 145-20, 145-25, 145-20-91
K051191 DCL MICROALBUMIN ASSAY, MODEL 252-20
K042330 ACETAMINOPHEN-SL ASSAY
K042329 SALICYLATE-SL ASSAY
K042362 MODIFICATION TO CARBON DIOXIDE-L3K ASSAY, CAT. NOS. 299-30, 299-17, 299-50, 299-80 AND 299-12
K041928 HDL-ADVANCE ASSAY, CAT. NO. 278-20, 278-50A, 278-50B
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