Cleared Traditional

K862802 - MULTI-CHANNEL MICROPIPETTES

K862802 is the FDA 510(k) clearance for MULTI-CHANNEL MICROPIPETTES by Dynatech Laboratories, Inc.. It is a Class 1 Hematology device (product code JTC) cleared through the Traditional 510(k) pathway after a 10-day FDA review.

K862802 · Dynatech Laboratories, Inc. · Hematology device
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Aug 1986
Decision
10d
Days
Class 1
Risk

K862802 is an FDA 510(k) clearance for the MULTI-CHANNEL MICROPIPETTES. Classified as Device, Microtiter Diluting/dispensing (product code JTC), Class I - General Controls.

Submitted by Dynatech Laboratories, Inc. (Chantilly, US). The FDA issued a Cleared decision on August 1, 1986 after a review of 10 days - a notably fast clearance cycle.

This device falls under the Hematology FDA review panel, regulated under 21 CFR 866.2500 - the FDA hematology 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 Laboratories, Inc. devices

Submission Details

510(k) Number K862802 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 22, 1986
Decision Date August 01, 1986
Days to Decision 10 days
Submission Type Traditional
Review Panel Hematology (HE)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
103d faster than avg
Panel avg: 113d · This submission: 10d
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 29
Devices cleared under the same product code (JTC) and FDA review panel - the closest regulatory comparables to K862802.
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K853920 · Bio-Tek Instruments, Inc. · Oct 1985
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K850908 · Flow Laboratories, Inc. · Mar 1985