Gelscan Software 2190

FDA 510(k) K834490 · Lkb Instruments, Inc.

Substantially Equivalent

510(k) numberK834490

Submission

Device name
Gelscan Software 2190
Applicant
Lkb Instruments, Inc.
Mchenry, IL, US
Received
December 6, 1983
Decision date
May 1, 1984
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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Questions and answers

When was Gelscan Software 2190 cleared by the FDA?

Gelscan Software 2190 (K834490) received a 510(k) decision of Substantially Equivalent on May 1, 1984, 147 days after the submission was received.

What is the product code of K834490?

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.