Stain, R-250, Coomassie Brilliant Blue

FDA 510(k) K770718 · Kallestad Laboratories, Inc.

Substantially Equivalent

510(k) numberK770718

Submission

Device name
Stain, R-250, Coomassie Brilliant Blue
Applicant
Kallestad Laboratories, Inc.
Mchenry, IL, US
Received
April 18, 1977
Decision date
April 26, 1977
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
JZS – Electrophoresis Instrumentation
Device class
Class I (low risk)
Regulation
21 CFR 866.4500
Specialty
Immunology

Other 510(k)s with product code JZS

510(k)DeviceApplicantDecision
K933123Synelisa TG Antibodies/Tpo AntibodiesJZS · Traditional Elias U.S.A., Inc.08/23/1993SE
K812194Immunodiffusion Band Intensifying FluidJZS · Traditional American Scientific Products08/31/1981SE
K770566Immunoelectrophoresis Profile KitJZS · Traditional Kallestad Laboratories, Inc.04/27/1977SE
K770719Immunoelectrofilm KihJZS · Traditional Kallestad Laboratories, Inc.04/26/1977SE
K770150Electro Immuno Assay KitJZS · Traditional Millipore Corp.02/01/1977SE

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K855014Quantimetric Plus Calibrator/Control Set aJIX · Traditional 03/14/1986SE
K855010Quantimetric Plus Igm Reagent KitDFT · Traditional 02/28/1986SE
K855013Quantimetric Plus Support PackDEH · Traditional 02/26/1986SE
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Questions and answers

When was Stain, R-250, Coomassie Brilliant Blue cleared by the FDA?

Stain, R-250, Coomassie Brilliant Blue (K770718) received a 510(k) decision of Substantially Equivalent on April 26, 1977, 8 days after the submission was received.

What is the product code of K770718?

The FDA product code is JZS – Electrophoresis Instrumentation, a Class I (low risk) device regulated under 21 CFR 866.4500.