Il 8060 Data Management System

FDA 510(k) K820427 · Instrumentation Laboratory CO

Substantially Equivalent

510(k) numberK820427

Submission

Device name
Il 8060 Data Management System
Applicant
Instrumentation Laboratory CO
Mchenry, IL, US
Received
February 17, 1982
Decision date
March 11, 1982
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
JQP – Calculator/Data Processing Module, For Clinical Use
Device class
Class I (low risk)
Regulation
21 CFR 862.2100
Specialty
Clinical Chemistry

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K113007Bionime Diabetes Management System VI.0JQP · Traditional Bionime Corporation02/27/2012SE
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K964460The RoboliteJQP · Traditional Shai Syg Motion and Innovations, Ltd.01/24/1997SE
K953652Prenval IJQP · Traditional Base Ten Systems, Inc.09/15/1995SE
K934111MR7000 with Time Manager Software (TMS)JQP · Traditional Dynatech Laboratories, Inc.11/02/1994SE
K923316Expresso CartridgeJQP · Traditional Bio-Rad Laboratories, Inc.02/23/1993SE
K893838Modified Model 570 Clinical Chemistry AnalyzerJQP · Traditional Ciba Corning Diagnostics Corp.08/31/1989SE
K892060Cyberlab High Volume Drug Testing SystemJQP · Traditional Syva Co.08/10/1989SE
K885292Cobas MFCJQP · Traditional Roche Diagnostic Systems, Inc.03/22/1989SE
K881194Ria-QuickJQP · Traditional Quantitative Technologies, Inc.06/01/1988SE

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Questions and answers

When was Il 8060 Data Management System cleared by the FDA?

Il 8060 Data Management System (K820427) received a 510(k) decision of Substantially Equivalent on March 11, 1982, 22 days after the submission was received.

What is the product code of K820427?

The FDA product code is JQP – Calculator/Data Processing Module, For Clinical Use, a Class I (low risk) device regulated under 21 CFR 862.2100.