AUTODILUTER 2

Station, Pipetting And Diluting, For Clinical Use

DYNATECH LABORATORIES, INC.

The following data is part of a premarket notification filed by Dynatech Laboratories, Inc. with the FDA for Autodiluter 2.

Pre-market Notification Details

Device IDK781645
510k NumberK781645
Device Name:AUTODILUTER 2
ClassificationStation, Pipetting And Diluting, For Clinical Use
Applicant DYNATECH LABORATORIES, INC. 803 N. Front St. Suite 3 Mchenry,  IL  60050
Product CodeJQW  
CFR Regulation Number862.2750 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1978-09-25
Decision Date1978-10-27

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