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510(k) K841146

NCS RA LATEX TEST by Ncs Diagnostics, Inc. — Product Code DHR

K841146 is an FDA 510(k) premarket notification submitted by Ncs Diagnostics, Inc. for the device "NCS RA LATEX TEST". The FDA issued a decision of Substantially Equivalent on April 20, 1984. The device falls under product code DHR (System, Test, Rheumatoid Factor), a Class II device regulated under 21 CFR 866.5775. Ncs Diagnostics, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 20, 1984
Date Received
March 16, 1984
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
System, Test, Rheumatoid Factor
Device Class
Class II
Regulation Number
866.5775
Review Panel
IM
Submission Type

Other clearances by Ncs Diagnostics, Inc.

  • K943498 — KULTSURE STARSWAB (M210), MODIFICATION (November 30, 1994)
  • K943499 — KULTSURE STARSWAB(M240), MODIFICATION (November 30, 1994)
  • K882811 — STREPSLIDE (October 25, 1988)
  • K881209 — ASO SLIDE TEST (April 12, 1988)
  • K874019 — STAPHSLIDE (October 28, 1987)
  • K871404 — KULTSURE (April 21, 1987)
  • K870231 — KULTSURE (February 4, 1987)
  • K860178 — KULTSURE (CULTURE TRANSPORT) (April 4, 1986)
  • K860655 — KULTSURE (CATALOGUE NO. M200) (March 6, 1986)
  • K860657 — KULTSURE (CATALOGUE NO. M240) (March 4, 1986)

Other clearances for product code DHR

  • K192727 — K-ASSAY (R) RF (Ver.2), K-ASSAY (R) RF Calibrator (Ver.2) (May 20, 2020)
  • K190088 — QUANTA Flash RF IgM Reagents, QUANTA Flash RF IgA Reagents (April 17, 2019)
  • K182747 — EliA RF IgM Immunoassay (December 18, 2018)
  • K162263 — Optilite Rheumatoid Factor Kit (May 3, 2017)
  • K160070 — Rheumatoid Factor (RF) Kit for use on SPAPLUS (December 7, 2016)
  • K143736 — ImmuLisa Enhanced RF IgA Antibody ELISA, ImmuLisa Enhanced RF IgG Antibody ELISA (September 23, 2015)
  • K102673 — RHEUMATOID FACTOR IMMUNOLOGICAL TEST SYSTEM (September 30, 2011)
  • K100499 — ORGENTEC RHEUMATOID FACTOR EIA (October 27, 2010)
  • K083080 — IGX PLEX RHEUMATOID ARTHRITIS (RA) ASSAY AND SQIDWORKS DIAGNOSTICS PLATFORM (October 29, 2009)
  • K071247 — N LATEX RF KIT (August 8, 2007)

FDA data resources