Cleared Traditional

K831364 - TESTCORP RA

K831364 is the FDA 510(k) clearance for TESTCORP RA by Myo-Tronics Research, Inc.. It is a Class 2 Microbiology device (product code DCN) cleared through the Traditional 510(k) pathway after a 31-day FDA review.

K831364 · Myo-Tronics Research, Inc. · Microbiology device
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May 1983
Decision
31d
Days
Class 2
Risk

K831364 is an FDA 510(k) clearance for the TESTCORP RA. Classified as System, Test, C-reactive Protein (product code DCN), Class II - Special Controls.

Submitted by Myo-Tronics Research, Inc. (Walker, US). The FDA issued a Cleared decision on May 27, 1983 after a review of 31 days - a notably fast clearance cycle.

This device falls under the Microbiology FDA review panel, regulated under 21 CFR 866.5270 - 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 Myo-Tronics Research, Inc. devices

Submission Details

510(k) Number K831364 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 26, 1983
Decision Date May 27, 1983
Days to Decision 31 days
Submission Type Traditional
Review Panel Microbiology (MI)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
71d faster than avg
Panel avg: 102d · This submission: 31d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code DCN System, Test, C-reactive Protein
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 866.5270
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 Microbiology devices follow this clearance model.

Regulatory Peers - DCN System, Test, C-reactive Protein

All 38
Devices cleared under the same product code (DCN) and FDA review panel - the closest regulatory comparables to K831364.
CPR SLIDE EIKEN
K854819 · Syn-Kit, Inc. · Feb 1986
LASER CRP KIT(C-REACTIVE PROTEIN REAGENTS)
K855057 · Behring Diagnostics, Inc. · Feb 1986
CRP SLIDE TEST KIT
K840699 · Difco Laboratories, Inc. · Mar 1984
EMIT C-REACTIVE PROTEIN ASSAY
K821413 · Syva Co. · May 1982
IMMUNEX CRP
K812881 · Armkel, LLC · Oct 1981
CRP SLIDE
K810862 · Syn-Kit, Inc. · Apr 1981