Kodak Ektachem Clinical Chemistry Slides (Li)

FDA 510(k) K924488 · Eastman Kodak Company

Substantially Equivalent

510(k) numberK924488

Submission

Device name
Kodak Ektachem Clinical Chemistry Slides (Li)
Applicant
Eastman Kodak Company
Rochester, NY, US
Received
September 3, 1992
Decision date
January 26, 1993
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
JIH – Flame Photometry, Lithium
Device class
Class II (moderate risk)
Regulation
21 CFR 862.3560
Specialty
Clinical Toxicology

Other 510(k)s with product code JIH

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K050338Modification to: Instaread Lithium SystemJIH · Special Akers Biosciences, Inc.03/04/2005SE
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K011033Dimension Lithium (Li) Flex Reagent Cartridge, Model DF 132JIH · Traditional Dade Behring, Inc.06/07/2001SE
K934106Kodak Ektachem DTSC II Slides (Li)JIH · Traditional Eastman Kodak Company04/25/1994SE
K921403Model 654 AnalyzerJIH · Traditional Ciba Corning Diagnostics Corp.07/30/1992SE
K895465Amdev Lytening 2Z Sodium/Potassium/Lithium AnalyzeJIH · Traditional Baxter Healthcare Corp12/27/1989SE
K894328Tdx(R) Lites(Tm) LithiumJIH · Traditional Abbott Laboratories11/13/1989SE
K830636Potassium DiluentJIH · Traditional Shaban Mfg. Co.04/05/1983SE
K800039Lithium Diluent (1500 Mm/E)JIH · Traditional Gilford Diagnostics01/21/1980SE
K771303Flame Photometer Model 460JIH · Traditional Corning Medical & Scientific08/22/1977SE

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Questions and answers

When was Kodak Ektachem Clinical Chemistry Slides (Li) cleared by the FDA?

Kodak Ektachem Clinical Chemistry Slides (Li) (K924488) received a 510(k) decision of Substantially Equivalent on January 26, 1993, 145 days after the submission was received.

What is the product code of K924488?

The FDA product code is JIH – Flame Photometry, Lithium, a Class II (moderate risk) device regulated under 21 CFR 862.3560.