Cleared Traditional

QUANTIMETRIX URINALYSIS MICROSCOPICS CONTROL

K925256 · Quantimetrix Corp. · Hematology
Mar 1993
Decision
133d
Days
Class 1
Risk

About This 510(k) Submission

K925256 is an FDA 510(k) clearance for the QUANTIMETRIX URINALYSIS MICROSCOPICS CONTROL, a Multi-analyte Controls, All Kinds (assayed) (Class I — General Controls, product code JJY), submitted by Quantimetrix Corp. (Hawthorne, US). The FDA issued a Cleared decision on March 1, 1993, 133 days after receiving the submission on October 19, 1992. This device falls under the Hematology review panel. Regulated under 21 CFR 862.1660.

Submission Details

510(k) Number K925256 FDA.gov
FDA Decision Cleared SESE
Date Received October 19, 1992
Decision Date March 01, 1993
Days to Decision 133 days
Submission Type Traditional
Review Panel Hematology (HE)
Summary Statement

Device Classification

Product Code JJY — Multi-analyte Controls, All Kinds (assayed)
Device Class Class I — General Controls
CFR Regulation 21 CFR 862.1660

Similar Devices — JJY Multi-analyte Controls, All Kinds (assayed)

All 672
Multichem IA Plus
K162530 · Techno-Path Manufacturing · Mar 2017
Audit MicroControls Linearity FD Tumor Markers II
K163629 · Aalto Scientific, Ltd. · Mar 2017
Liquichek Tumor Marker Control-Level 1; Liquichek Tumor Marker Control-Level 2; Liquichek Tumor Marker Control-Level 3; Liquichek Tumor Marker Control- Trilevel MiniPak
K163015 · Bio-Rad Laboratories · Jan 2017
VK-3 Verification Kit, VK-4 Verification Kit, VK-R5 Verification Kit, VK-R7 Verification Kit, VK-Crea Verification Kit
K153712 · Radiometer America, Inc. · Jan 2016
Liquichek Cardiac Markers Plus Control LT
K150300 · Bio-Rad Laboratories · Dec 2015
VALIDATE Anemia Calibration Verification/ Linearity Test Kit
K142964 · Maine Standards Company, LLC · Apr 2015