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

RF DIPSTICK TEST KIT

K Number: K874151 · Decision Dec 29, 1987
Classifications
1
FEI Numbers
57
Registration Numbers
57
Same Product Code
143
Applicant Total
15
Review Days
77

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
RF DIPSTICK TEST KIT
K Number
K874151
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5775
Medical Specialty
Immunology
Decision
Substantially Equivalent
Applicant
Lipogen, Inc.
Date Received
October 13, 1987
Decision Date
December 29, 1987
Product Code
DHR
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
DHR System, Test, Rheumatoid Factor

Similar 510(k) Clearances

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

View all

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
K880254 SM ANTIBODY TEST KIT
Search all 15 clearances from Lipogen, Inc. →