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

SM ANTIBODY TEST KIT

K Number: K880254 · Decision Apr 6, 1988
Classifications
1
FEI Numbers
17
Registration Numbers
17
Same Product Code
27
Applicant Total
15
Review Days
77

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Basic Information

Device Name
SM ANTIBODY TEST KIT
K Number
K880254
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5100
Medical Specialty
Immunology
Decision
Substantially Equivalent
Applicant
Lipogen, Inc.
Date Received
January 20, 1988
Decision Date
April 6, 1988
Product Code
LKP
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
LKP Anti-Sm Antibody, Antigen And Control

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Other Clearances by Lipogen, Inc.

K Number Device Name
K902636 LIPOGEN RHEUMELISA DSDNA ASSAY
K895997 RHEUMELISA ASSAY FOR RNP AUTOANTIBODIES
K895996 RHEUMELISA ASSAY FOR SM AUTOANTIBODIES
K895995 RHEUMELISA ASSAY FOR SS-B/LA AUTOANTIBODIES
K895994 RHEUMELISA ASSAY FOR SS-A/RO AUTOANTIBODIES
K894659 ANA ANTISERA CONTROL KIT
K892421 MODIFIED ACCESS R-CLONE ANA/RF SCREENING TEST
K885048 ACCESS R-CLONE ANA PROFILE ASSAY
K882740 ACCESS R-CLONE(TM) ANA/RF SCREENING ASSAY
K874152 RNP ANTIBODY TEST KIT
Search all 15 clearances from Lipogen, Inc. →