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

THE THERATEST EL-ANA PROFILES: ANTI-CENTROMERE

K Number: K024031 · Decision Feb 6, 2003
Classifications
1
FEI Numbers
26
Registration Numbers
26
Same Product Code
111
Applicant Total
22
Review Days
62

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Basic Information

Device Name
THE THERATEST EL-ANA PROFILES: ANTI-CENTROMERE
K Number
K024031
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5100
Medical Specialty
Immunology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Theratest Laboratories, Inc.
Date Received
December 6, 2002
Decision Date
February 6, 2003
Product Code
LJM
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
LJM Antinuclear Antibody (Enzyme-Labeled), Antigen, Controls

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Other Clearances by Theratest Laboratories, Inc.

K Number Device Name
K090753 THERATEST EL-ANTI-CCP/2
K090760 THERATEST EL-ANTI-TPO AND THERATEST EL-ANTI-THYROGLOBULIN, MODEL 104-119, 103-120
K071692 THERATEST EL-TTG IGA/IGG AND THERATEST EL-GLIA IGA/IGG TEST SYSTEMS
K061376 EL-ANCA: ANTI-MPO, ANTI-PR3, ANTI-MPO AND ANTI-PR3
K060176 EL-ACL SCREEN; EL-ACL IGM, IGG, IGA
K051066 THERATEST EL-ANA PROFILES
K040291 EL-ANA PROFILES: ANTI-CHROMATIN
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. →