Cleared Traditional

DIGITAL DISPENSING PUMP

K810509 · Dynatech Corp. · Chemistry
Mar 1981
Decision
10d
Days
Class 1
Risk

About This 510(k) Submission

K810509 is an FDA 510(k) clearance for the DIGITAL DISPENSING PUMP, a Station, Pipetting And Diluting, For Clinical Use (Class I — General Controls, product code JQW), submitted by Dynatech Corp. (Mchenry, US). The FDA issued a Cleared decision on March 6, 1981, 10 days after receiving the submission on February 24, 1981. This device falls under the Chemistry review panel. Regulated under 21 CFR 862.2750.

Submission Details

510(k) Number K810509 FDA.gov
FDA Decision Cleared SESE
Date Received February 24, 1981
Decision Date March 06, 1981
Days to Decision 10 days
Submission Type Traditional
Review Panel Chemistry (CH)
Summary —

Device Classification

Product Code JQW — Station, Pipetting And Diluting, For Clinical Use
Device Class Class I — General Controls
CFR Regulation 21 CFR 862.2750

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