Agarose Barbital Buffer

FDA 510(k) K792547 · Electrophoresis Corp. of America

Substantially Equivalent

510(k) numberK792547

Submission

Device name
Agarose Barbital Buffer
Applicant
Electrophoresis Corp. of America
Mchenry, IL, US
Received
December 10, 1979
Decision date
January 29, 1980
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

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

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K881852Rep SP Electrophoresis System Cat No. 3170JJN · Traditional Helena Laboratories07/08/1988SE
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K873352Rapid Electrophoresis System (Rep)JJN · Traditional Helena Laboratories09/08/1987SE
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K861414Electrophoresis Work Center (Ewc)JJN · Traditional Helena Laboratories08/26/1986SE
K841407Isogel AgaroseJJN · Traditional Fmc Corp.07/16/1985SE
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More from Logos Scientific, Inc.

510(k)DeviceDecision
K802396General Procedure Agarose FilmJJN · Traditional 11/26/1980SE
K792553Agarose Barbital-Edta BufferJJN · Traditional 01/29/1980SE
K792551Alkaline Phosphatase ReagentCJH · Traditional 01/29/1980SE
K792548Alkaline Phosphatase MarkerCIN · Traditional 01/29/1980SE
K792574Mopso BufferJCC · Traditional 01/21/1980SE
K792550Ponceau S Stain SetKQC · Traditional 01/16/1980SE
K792552Amido Black 10B StainHZZ · Traditional 12/18/1979SE
K792549Fat Red 7B Stain SetHYD · Traditional 12/18/1979SE
K791657LDH Isoenzyme ReagentCFE · Traditional 09/17/1979SE
K791656Enzyme Stabilizing Reagent (Esr)CFE · Traditional 09/17/1979SE

Questions and answers

When was Agarose Barbital Buffer cleared by the FDA?

Agarose Barbital Buffer (K792547) received a 510(k) decision of Substantially Equivalent on January 29, 1980, 50 days after the submission was received.

What is the product code of K792547?

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