MS-2 Identification System

FDA 510(k) K802309 · Abbott Laboratories

Substantially Equivalent

510(k) numberK802309

Submission

Device name
MS-2 Identification System
Applicant
Abbott Laboratories
Abbott Park, IL, US
Received
September 23, 1980
Decision date
December 1, 1980
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
JXB – Kit, Identification, Yeast
Device class
Class I (low risk)
Regulation
21 CFR 866.2660
Specialty
Microbiology

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K080719Yeast Traffic Light Pna FishJXB · Traditional Advandx, Inc.09/12/2008SE
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K993554YeastestJXB · Traditional Diagnostic Markers, Inc.02/10/2000SE
K943621Rapid Yeast Plus SystemJXB · Traditional Innovative Diagnostic Systems, Inc.01/27/1995SE
K935124Bacticard CandidaJXB · Traditional Remel Co.02/25/1994SE
K900112Microring YtJXB · Traditional Medical Wire & Equipment Co.07/31/1990SE
K881925Vitek Yeast Biochemical CardJXB · Traditional Vitek Systems, Inc.06/16/1988SE
K860575Yeast Identification PanelJXB · Traditional American Micro Scan05/13/1986SE
K830286Yeast IdentJXB · Traditional Analytical Products, Inc.04/05/1983SE
K800803Nitrate Swab-Rapid TestJXB · Traditional Remel Co.07/08/1980SE

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Questions and answers

When was MS-2 Identification System cleared by the FDA?

MS-2 Identification System (K802309) received a 510(k) decision of Substantially Equivalent on December 1, 1980, 69 days after the submission was received.

What is the product code of K802309?

The FDA product code is JXB – Kit, Identification, Yeast, a Class I (low risk) device regulated under 21 CFR 866.2660.