FDA 510(k) FDA class 2 Substantially Equivalent 🇮🇪 Ireland

RANDOX COMPLEMENT C3

K Number: K000469 · Decision Mar 27, 2000
Classifications
1
FEI Numbers
32
Registration Numbers
32
Same Product Code
43
Applicant Total
116
Review Days
45

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Basic Information

Device Name
RANDOX COMPLEMENT C3
K Number
K000469
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5240
Medical Specialty
Immunology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Randox Laboratories, Ltd.
Date Received
February 11, 2000
Decision Date
March 27, 2000
Product Code
CZW
Advisory Committee
Immunology
Review Advisory Committee
IM
Third Party
N

Classifications

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

Product Code Device Name
CZW Complement C3, Antigen, Antiserum, Control

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