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

ACCESS R-CLONE(TM) ANA/RF SCREENING ASSAY

K Number: K882740 · Decision Sep 22, 1988
Classifications
1
FEI Numbers
16
Registration Numbers
16
Same Product Code
49
Applicant Total
15
Review Days
83

Basic Information

Device Name
ACCESS R-CLONE(TM) ANA/RF SCREENING ASSAY
K Number
K882740
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5100
Medical Specialty
Immunology
Decision
Substantially Equivalent
Applicant
LIPOGEN, INC.
Date Received
July 1, 1988
Decision Date
September 22, 1988
Product Code
LKJ
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
LKJ Antinuclear Antibody, Antigen, Control

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (LKJ), ordered by most recent decision date.

View all

Other Clearances by LIPOGEN, INC.

K Number Device Name
K902636 LIPOGEN RHEUMELISA DSDNA ASSAY
K895996 RHEUMELISA ASSAY FOR SM AUTOANTIBODIES
K895997 RHEUMELISA ASSAY FOR RNP 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
K880254 SM ANTIBODY TEST KIT
K874152 RNP ANTIBODY TEST KIT
Search all 15 clearances from LIPOGEN, INC. →