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

HEMOSIL ACUSTAR ANTI-B2 GLYCOPROTEIN-I; IGG, IGM, IGG CONTROLS, IGM CONTROLS

K Number: K091556 · Decision May 21, 2010
Classifications
1
FEI Numbers
19
Registration Numbers
19
Same Product Code
45
Applicant Total
321
Review Days
359

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Basic Information

Device Name
HEMOSIL ACUSTAR ANTI-B2 GLYCOPROTEIN-I; IGG, IGM, IGG CONTROLS, IGM CONTROLS
K Number
K091556
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5660
Medical Specialty
Immunology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Instrumentation Laboratory CO
Date Received
May 27, 2009
Decision Date
May 21, 2010
Product Code
MSV
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
MSV System,Test,Antibodies,B2 - Glycoprotein I (B2 - Gpi)

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