Autoreader Calibration Test Plate

FDA 510(k) K900579 · Bio-Tek Instruments, Inc.

Substantially Equivalent

510(k) numberK900579

Submission

Device name
Autoreader Calibration Test Plate
Applicant
Bio-Tek Instruments, Inc.
Winooski, VT, US
Received
February 7, 1990
Decision date
February 27, 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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Questions and answers

When was Autoreader Calibration Test Plate cleared by the FDA?

Autoreader Calibration Test Plate (K900579) received a 510(k) decision of Substantially Equivalent on February 27, 1990, 20 days after the submission was received.

What is the product code of K900579?

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