Biowhittaker 2001 Microplate Reader Firmware

FDA 510(k) K942245 · Biowhittaker Molecular Applications, Inc.

Substantially Equivalent

510(k) numberK942245

Submission

Device name
Biowhittaker 2001 Microplate Reader Firmware
Applicant
Biowhittaker Molecular Applications, Inc.
Walkersville, MD, US
Received
May 9, 1994
Decision date
April 3, 1995
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

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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K973938Alpha 4 LS Automated Microtiterplate Processor and ReaderJJQ · Traditional Sfri, Inc.02/04/1998SE
K974762Stat TracksJJQ · Traditional Awareness Technology, Inc.01/28/1998SE
K962113Anthos Phacts Version Microplate ReaderJJQ · Traditional Columbia Bioscience, Inc.11/05/1996SE
K961183Cbi 7520 ReaderJJQ · Traditional Columbia Bioscience, Inc.08/02/1996SE
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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Questions and answers

When was Biowhittaker 2001 Microplate Reader Firmware cleared by the FDA?

Biowhittaker 2001 Microplate Reader Firmware (K942245) received a 510(k) decision of Substantially Equivalent on April 3, 1995, 329 days after the submission was received.

What is the product code of K942245?

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