Electrophoresis Tank

FDA 510(k) K924020 · The Binding Site, Ltd.

Substantially Equivalent

510(k) numberK924020

Submission

Device name
Electrophoresis Tank
Applicant
The Binding Site, Ltd.
Los Angeles, CA, US
Received
August 11, 1992
Decision date
December 28, 1992
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
JJN – Apparatus, Electrophoresis, For Clinical Use
Device class
Class I (low risk)
Regulation
21 CFR 862.2485
Specialty
Clinical Chemistry

Other 510(k)s with product code JJN

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K924021Power SupplyJJN · Traditional The Binding Site, Ltd.01/28/1993SE
K882344Electr-TransblotterJJN · Traditional The W.E.P. Co.01/13/1989SE
K881852Rep SP Electrophoresis System Cat No. 3170JJN · Traditional Helena Laboratories07/08/1988SE
K882163Helena Rep Gel ProcessorJJN · Traditional Helena Laboratories06/20/1988SE
K873352Rapid Electrophoresis System (Rep)JJN · Traditional Helena Laboratories09/08/1987SE
K864436Stavip 3000JJN · Traditional Roseburg SA03/16/1987SE
K861414Electrophoresis Work Center (Ewc)JJN · Traditional Helena Laboratories08/26/1986SE
K841407Isogel AgaroseJJN · Traditional Fmc Corp.07/16/1985SE
K844710Eurochima Serum Protein Electrophoresis MethodJJN · Traditional Logos Scientific, Inc.01/07/1985SE
K842560OPTIPHOR-10JJN · Traditional Gelman Sciences, Inc.08/10/1984SE

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Questions and answers

When was Electrophoresis Tank cleared by the FDA?

Electrophoresis Tank (K924020) received a 510(k) decision of Substantially Equivalent on December 28, 1992, 139 days after the submission was received.

What is the product code of K924020?

The FDA product code is JJN – Apparatus, Electrophoresis, For Clinical Use, a Class I (low risk) device regulated under 21 CFR 862.2485.