Il #781, Semi-Automated Loader

FDA 510(k) K811696 · Instrumentation Laboratory CO

Substantially Equivalent

510(k) numberK811696

Submission

Device name
Il #781, Semi-Automated Loader
Applicant
Instrumentation Laboratory CO
Mchenry, IL, US
Received
June 16, 1981
Decision date
July 1, 1981
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
JQW – Station, Pipetting And Diluting, For Clinical Use
Device class
Class I (low risk)
Regulation
21 CFR 862.2750
Specialty
Clinical Chemistry

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K9801802700 Sample ManagerJQW · Traditional Waters Corporation02/12/1998SE
K970420Mastercap Am 5.0/MASTERCAP RM 5.0JQW · Traditional Pharmacia, Inc.06/30/1997SE
K970616Mini Sampler ProcessorJQW · Traditional Cavro Scientific Instruments, Inc.04/21/1997SE
K962687Gio. de Vita E C. S.R.L.(Gdv) Automatic Washing SystemJQW · Traditional Nichols Institute Diagnostics03/28/1997SE
K962859Mini Sample ProcessorJQW · Traditional Cavro Scientific Instruments, Inc.10/29/1996SE
K961896Microlab 4000, Microlab 4200JQW · Traditional Hamilton Co.08/16/1996SE
K961694ImpactJQW · Traditional Matrix Technologies Corp.06/21/1996SE
K953345GenesisJQW · Traditional Tecan U.S., Inc.11/21/1995SE

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Questions and answers

When was Il #781, Semi-Automated Loader cleared by the FDA?

Il #781, Semi-Automated Loader (K811696) received a 510(k) decision of Substantially Equivalent on July 1, 1981, 15 days after the submission was received.

What is the product code of K811696?

The FDA product code is JQW – Station, Pipetting And Diluting, For Clinical Use, a Class I (low risk) device regulated under 21 CFR 862.2750.