Cleared Traditional

AUTODILUTER III

K810659 · Dynatech Corp. · Toxicology
Mar 1981
Decision
20d
Days
Class 1
Risk

About This 510(k) Submission

K810659 is an FDA 510(k) clearance for the AUTODILUTER III, a Device, Microtiter Diluting/dispensing (Class I — General Controls, product code JTC), submitted by Dynatech Corp. (Mchenry, US). The FDA issued a Cleared decision on March 31, 1981, 20 days after receiving the submission on March 11, 1981. This device falls under the Toxicology review panel. Regulated under 21 CFR 866.2500.

Submission Details

510(k) Number K810659 FDA.gov
FDA Decision Cleared SESE
Date Received March 11, 1981
Decision Date March 31, 1981
Days to Decision 20 days
Submission Type Traditional
Review Panel Toxicology (TX)
Summary —

Device Classification

Product Code JTC — Device, Microtiter Diluting/dispensing
Device Class Class I — General Controls
CFR Regulation 21 CFR 866.2500

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