The Yellow Iris Urinalysis Workstation

FDA 510(k) K972141 · Intl. Remote Imaging Systems

Substantially Equivalent

510(k) numberK972141

Submission

Device name
The Yellow Iris Urinalysis Workstation
Applicant
Intl. Remote Imaging Systems
Chatsworth, CA, US
Received
June 6, 1997
Decision date
August 25, 1997
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
KQO – Automated Urinalysis System
Device class
Class I (low risk)
Regulation
21 CFR 862.2900
Specialty
Clinical Chemistry

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More from ACON Laboratories, Inc.

510(k)DeviceDecision
K022774Iq 200 SystemLKM · Traditional 10/21/2002SE
K000373939UDX Urine Pathology SystemLKM · Traditional 04/14/2000SE
K953116White Iris Leukocyte Differential AnalyzerGKZ · Traditional 05/13/1996SE
K960054900UDX Urine Pathology SystemKQO · Traditional 03/22/1996SE
K954006Yellow Iris Urinalysis Workstation W/Iriscope Body Fluid Analysis CapabilityGKL · Traditional 03/12/1996SE
K943463The Yellow IrisKQO · Traditional 09/20/1994SE
K934539The Yellow Iris Urinalysis Workstation with Iriscope Body Fluid Analysis CapabilityGKL · Traditional 03/30/1994SE
K914256Yellow Iris Urinalysis Wrksta W/Iriscope Bdy FluGKL · Traditional 05/01/1992SE
K893530Iristain Formula 2, Parts 1 and 2JTS · Traditional 06/13/1989SE
K874207The Purple Iris(Tm) Cytopathology WorkstationIBJ · Traditional 01/05/1988SE

Questions and answers

When was The Yellow Iris Urinalysis Workstation cleared by the FDA?

The Yellow Iris Urinalysis Workstation (K972141) received a 510(k) decision of Substantially Equivalent on August 25, 1997, 80 days after the submission was received.

What is the product code of K972141?

The FDA product code is KQO – Automated Urinalysis System, a Class I (low risk) device regulated under 21 CFR 862.2900.