Cleared Traditional

K820821 - MIC-2000 PLUS

K820821 is the FDA 510(k) clearance for MIC-2000 PLUS by Dynatech Corp.. It is a Class 1 Microbiology device (product code JTC) cleared through the Traditional 510(k) pathway after a 21-day FDA review.

Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Apr 1982
Decision
21d
Days
Class 1
Risk

K820821 is an FDA 510(k) clearance for the MIC-2000 PLUS, 96 CHANNEL DISPENSER. Classified as Device, Microtiter Diluting/dispensing (product code JTC), Class I - General Controls.

Submitted by Dynatech Corp. (Mchenry, US). The FDA issued a Cleared decision on April 14, 1982 after a review of 21 days - a notably fast clearance cycle.

This device falls under the Microbiology FDA review panel, regulated under 21 CFR 866.2500 - the FDA microbiology device framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

View all Dynatech Corp. devices

Submission Details

510(k) Number K820821 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 24, 1982
Decision Date April 14, 1982
Days to Decision 21 days
Submission Type Traditional
Review Panel Microbiology (MI)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
81d faster than avg
Panel avg: 102d · This submission: 21d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code JTC Device, Microtiter Diluting/dispensing
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 866.2500
What this classification means

Class I devices are subject to general controls only and most are exempt from 510(k) premarket notification. They represent the lowest regulatory burden in the FDA device framework.

Regulatory Peers - JTC Device, Microtiter Diluting/dispensing

All 30
Devices cleared under the same product code (JTC) and FDA review panel - the closest regulatory comparables to K820821.
API UNISCEPT PLUS AUTOINOCULATOR
K831341 · Analytical Products, Inc. · Jun 1983
MUELLER HINTON W/50% SHEEP BLOOD
K830059 · bioMerieux, Inc. · Feb 1983
DISPOSABLE DISPENSE MANIFOLD
K823218 · Dynatech Laboratories, Inc. · Nov 1982
TITERTEK AUTODROP
K812818 · Flow Laboratories, Inc. · Oct 1981
SCEPTOR SYSTEM AUTOMATED MODEL 216
K810229 · Bd Becton Dickinson Vacutainer Systems Preanalytic · Feb 1981
MICROMEDIC REAGENT DISPENSER
K803252 · Micromedic Systems · Jan 1981