MICROLITE MICROTITER PLATE LUMINOMETER ML2200

Fluorometer, For Clinical Use

DYNATECH LABORATORIES, INC.

The following data is part of a premarket notification filed by Dynatech Laboratories, Inc. with the FDA for Microlite Microtiter Plate Luminometer Ml2200.

Pre-market Notification Details

Device IDK920888
510k NumberK920888
Device Name:MICROLITE MICROTITER PLATE LUMINOMETER ML2200
ClassificationFluorometer, For Clinical Use
Applicant DYNATECH LABORATORIES, INC. 14340 SULLYFIELD CIRCLE Chantilly,  VA  22021
ContactWarren D Gehle
CorrespondentWarren D Gehle
DYNATECH LABORATORIES, INC. 14340 SULLYFIELD CIRCLE Chantilly,  VA  22021
Product CodeKHO  
CFR Regulation Number862.2560 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1992-02-11
Decision Date1992-03-19

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