Cleared Traditional

K830200 - MICROELISA MINIREADER II

K830200 is the FDA 510(k) clearance for MICROELISA MINIREADER II by Dynatech Corp.. It is a Class 2 Chemistry device (product code LBI) cleared through the Traditional 510(k) pathway after a 27-day FDA review.

K830200 · Dynatech Corp. · Chemistry device
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Feb 1983
Decision
27d
Days
Class 2
Risk

K830200 is an FDA 510(k) clearance for the MICROELISA MINIREADER II. Classified as Unit, Neonatal Phototherapy (product code LBI), Class II - Special Controls.

Submitted by Dynatech Corp. (Mchenry, US). The FDA issued a Cleared decision on February 16, 1983 after a review of 27 days - a notably fast clearance cycle.

This device falls under the Chemistry FDA review panel, regulated under 21 CFR 880.5700 - the FDA in vitro diagnostics and chemistry 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 K830200 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 20, 1983
Decision Date February 16, 1983
Days to Decision 27 days
Submission Type Traditional
Review Panel Chemistry (CH)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
61d faster than avg
Panel avg: 88d · This submission: 27d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code LBI Unit, Neonatal Phototherapy
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 880.5700
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most Chemistry devices follow this clearance model.

Regulatory Peers - LBI Unit, Neonatal Phototherapy

All 24
Devices cleared under the same product code (LBI) and FDA review panel - the closest regulatory comparables to K830200.
OLYMPIC BILI-LITE-PAD(TM)
K901987 · Olympic Medical Corp. · Jul 1990
BILIBLANKET PHOTOTHERAPY DEVICE
K894129 · Ohmeda Medical · Sep 1989
PHOTOTHERAPY UNIT 7850 NEONATAL PHOTO
K840454 · Air-Shields, Inc. · Mar 1984
NEONATAL PHOTOTHERAPY UNIT
K802702 · Ohio Medical Products · Dec 1980
BILI-DOSIMETER
K791114 · Olympic Medical Corp. · Sep 1979
PHOTOTHERAPY/PROCEDURE LAMP
K771025 · Cavitron Corp. · Oct 1977