Manual Micro Elisa Reader #2-530

FDA 510(k) K791302 · Dynatech Laboratories, Inc.

Substantially Equivalent

510(k) numberK791302

Submission

Device name
Manual Micro Elisa Reader #2-530
Applicant
Dynatech Laboratories, Inc.
Mchenry, IL, US
Received
July 10, 1979
Decision date
August 16, 1979
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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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

More from Bio-Tek Instruments, Inc.

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K943701MRX Microplate ReaderJJQ · Traditional 10/20/1994SE
K923456Microlite Microtiter Plate Luminometer ML3000JJQ · Traditional 10/13/1992SE
K915896Microlite Microtiter Plate Luminometer ML2250/MODIJJQ · Traditional 05/04/1992SE
K920888Microlite Microtiter Plate Luminometer ML2200KHO · Traditional 03/19/1992SE
K913590Microlite ML 1000 Microtiter Plate LuminometerJJQ · Traditional 10/25/1991SE
K895313Microlite ML 1000 (Model 3) Microplate LuminometerJJQ · Traditional 10/17/1989SE
K894645Immulon 1,2,3,AND 4 Dividastrips TMJTC · Traditional 10/17/1989SE
K894687Dynatech MR 5000, Catalog #011-976-0600JJQ · Traditional 08/31/1989SE

Questions and answers

When was Manual Micro Elisa Reader #2-530 cleared by the FDA?

Manual Micro Elisa Reader #2-530 (K791302) received a 510(k) decision of Substantially Equivalent on August 16, 1979, 37 days after the submission was received.

What is the product code of K791302?

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