MPR-4A - Micro-Plate Reader

FDA 510(k) K901965 · Tosoh Corp.

Substantially Equivalent

510(k) numberK901965

Submission

Device name
MPR-4A - Micro-Plate Reader
Applicant
Tosoh Corp.
Washington, D.C., DC, US
Received
April 30, 1990
Decision date
May 10, 1990
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
JJQ – Colorimeter, Photometer, Spectrophotometer For Clinical Use
Device class
Class I (low risk)
Regulation
21 CFR 862.2300
Specialty
Clinical Chemistry

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K962166Origen AnalyzerJJQ · Traditional Igen, Inc.07/31/1996SE
K955077Anthos 2010 ReaderJJQ · Traditional Anthos Labtec, Inc.12/04/1995SE
K953710ELX808 Automated Microplate ReadersJJQ · Traditional Bio-Tek Instruments, Inc.10/25/1995SE
K953572ELX800UVJJQ · Traditional Bio-Tek Instruments, Inc.10/19/1995SE

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K903628Aia-Pack IriCFP · Traditional 09/07/1990SE
K901674AIA-600 Automated Enzyme Immunoassay SystemKHO · Traditional 05/02/1990SE
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Questions and answers

When was MPR-4A - Micro-Plate Reader cleared by the FDA?

MPR-4A - Micro-Plate Reader (K901965) received a 510(k) decision of Substantially Equivalent on May 10, 1990, 10 days after the submission was received.

What is the product code of K901965?

The FDA product code is JJQ – Colorimeter, Photometer, Spectrophotometer For Clinical Use, a Class I (low risk) device regulated under 21 CFR 862.2300.