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

LIQUICHEK ANTI-DSDNA CONTROL, MODEL 213

K Number: K984396 · Decision Dec 18, 1998
Classifications
1
FEI Numbers
14
Registration Numbers
14
Same Product Code
28
Applicant Total
319
Review Days
9

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Basic Information

Device Name
LIQUICHEK ANTI-DSDNA CONTROL, MODEL 213
K Number
K984396
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5100
Medical Specialty
Immunology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Bio-Rad
Date Received
December 9, 1998
Decision Date
December 18, 1998
Product Code
LRM
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
LRM Anti-Dna Antibody (Enzyme-Labeled), Antigen, Control

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