Cleared Traditional

HEMOCHEK-A1C SAMPLE COLLECTION KIT

K990899 · Osborn Group, Inc. · Hematology
Dec 1999
Decision
278d
Days
Class 2
Risk

About This 510(k) Submission

K990899 is an FDA 510(k) clearance for the HEMOCHEK-A1C SAMPLE COLLECTION KIT, a Assay, Glycosylated Hemoglobin (Class II — Special Controls, product code LCP), submitted by Osborn Group, Inc. (Olathe, US). The FDA issued a Cleared decision on December 21, 1999, 278 days after receiving the submission on March 18, 1999. This device falls under the Hematology review panel. Regulated under 21 CFR 864.7470.

Submission Details

510(k) Number K990899 FDA.gov
FDA Decision Cleared SESE
Date Received March 18, 1999
Decision Date December 21, 1999
Days to Decision 278 days
Submission Type Traditional
Review Panel Hematology (HE)
Summary Summary PDF

Device Classification

Product Code LCP — Assay, Glycosylated Hemoglobin
Device Class Class II — Special Controls
CFR Regulation 21 CFR 864.7470

Similar Devices — LCP Assay, Glycosylated Hemoglobin

All 248
Nova Allegro HbA1c Assay, Nova Allegro Analyzer
K221326 · Nova Biomedical Corporation · Nov 2024
Q-Pad Test System
K231465 · Qurasense · Dec 2023
Afinion? HbA1c, Afinion? 2 and Alere Afinion? AS100 Analyzer
K214117 · Abbott Diagnostics Technologies AS · Sep 2023
Aina HbA1c Monitoring System 2
K192987 · Jana Care, Inc. · Mar 2020
PixoTest POCT System - PixoTest POCT Analyzer and PixoTest A1c Test Kit
K192369 · Ixensor Co, Ltd. · Oct 2019
OneDraw A1C Test System
K183230 · Drawbridge Health, Inc. · Aug 2019