Cleared Traditional

SRD III

K810022 · Dynatech Corp. · Chemistry
Jan 1981
Decision
21d
Days
Class 1
Risk

About This 510(k) Submission

K810022 is an FDA 510(k) clearance for the SRD 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 January 26, 1981, 21 days after receiving the submission on January 5, 1981. This device falls under the Chemistry review panel. Regulated under 21 CFR 866.2500.

Submission Details

510(k) Number K810022 FDA.gov
FDA Decision Cleared SESE
Date Received January 05, 1981
Decision Date January 26, 1981
Days to Decision 21 days
Submission Type Traditional
Review Panel Chemistry (CH)
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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