Cleared Traditional

SPQ(TM) ANTIBODY REAGENT SET II FOR IGA

K890560 · Atlantic Antibodies · Immunology
Feb 1989
Decision
22d
Days
Class 2
Risk

About This 510(k) Submission

K890560 is an FDA 510(k) clearance for the SPQ(TM) ANTIBODY REAGENT SET II FOR IGA, a Iga, Antigen, Antiserum, Control (Class II — Special Controls, product code CZP), submitted by Atlantic Antibodies (Scarborough, US). The FDA issued a Cleared decision on February 15, 1989, 22 days after receiving the submission on January 24, 1989. This device falls under the Immunology review panel. Regulated under 21 CFR 866.5510.

Submission Details

510(k) Number K890560 FDA.gov
FDA Decision Cleared SESE
Date Received January 24, 1989
Decision Date February 15, 1989
Days to Decision 22 days
Submission Type Traditional
Review Panel Immunology (IM)
Summary

Device Classification

Product Code CZP — Iga, Antigen, Antiserum, Control
Device Class Class II — Special Controls
CFR Regulation 21 CFR 866.5510

Similar Devices — CZP Iga, Antigen, Antiserum, Control

All 53
Yumizen C1200 Immunoglobulin A, Yumizen C1200 Immunoglobulin G, Yumizen C1200 Immunoglobulin M
K193525 · HORIBA ABX SAS · Jun 2020
IMMAGE SYSTEMS LOW CONCENTRATION IMMUNOGLOBULIN A REAGENT
K060130 · Beckman Coulter, Inc. · Feb 2006
ROCHE DIAGNOSTICS TINA-QUANT IGA GEN.2
K040435 · Roche Diagnostics Corp. · Mar 2004
N LATEX IGA
K024038 · Dade Behring, Inc. · Feb 2003
WAKO IGA II-HA, IMMUNOGLOBULIN CALIBRATOR SET, IMMUNOGLOBULIN STANDRAD
K993927 · Wako Chemicals USA, Inc. · Jan 2000
IGA
K983359 · Abbott Laboratories · Nov 1998