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

EL-ANCA: ANTI-MPO, ANTI-PR3, ANTI-MPO AND ANTI-PR3

K Number: K061376 · Decision Jul 20, 2006
Classifications
1
FEI Numbers
26
Registration Numbers
26
Same Product Code
73
Applicant Total
22
Review Days
64

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Basic Information

Device Name
EL-ANCA: ANTI-MPO, ANTI-PR3, ANTI-MPO AND ANTI-PR3
K Number
K061376
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5660
Medical Specialty
Immunology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Theratest Laboratories, Inc.
Date Received
May 17, 2006
Decision Date
July 20, 2006
Product Code
MOB
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
MOB Test System, Antineutrophil Cytoplasmic Antibodies (Anca)

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Other Clearances by Theratest Laboratories, Inc.

K Number Device Name
K090753 THERATEST EL-ANTI-CCP/2
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K071692 THERATEST EL-TTG IGA/IGG AND THERATEST EL-GLIA IGA/IGG TEST SYSTEMS
K060176 EL-ACL SCREEN; EL-ACL IGM, IGG, IGA
K051066 THERATEST EL-ANA PROFILES
K040291 EL-ANA PROFILES: ANTI-CHROMATIN
K024031 THE THERATEST EL-ANA PROFILES: ANTI-CENTROMERE
K024151 EL-ANA PROFILES: ANTI-RIBOSOMAL PROTEIN P
K002559 EL-ANA PROFILES-2K1
K982622 EL-ANA PROFILES: EL-ENA/5
Search all 22 clearances from Theratest Laboratories, Inc. →