Cleared Traditional

K053243 - SENSITITRE 18-24 HOURS SUSCEPTIBILITY P...

K053243 is the FDA 510(k) clearance for SENSITITRE 18-24 HOURS SUSCEPTIBILITY P... by Trek Diagnostic Systems, Inc.. It is a Class 2 Microbiology device (product code LRG) cleared through the Traditional 510(k) pathway after a 60-day FDA review.

K053243 · Trek Diagnostic Systems, Inc. · Microbiology device
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Jan 2006
Decision
60d
Days
Class 2
Risk

K053243 is an FDA 510(k) clearance for the SENSITITRE 18-24 HOURS SUSCEPTIBILITY PLATES. Classified as Instrument For Auto Reader & Interpretation Of Overnight Suscept. Systems (product code LRG), Class II - Special Controls.

Submitted by Trek Diagnostic Systems, Inc. (Cleveland, US). The FDA issued a Cleared decision on January 20, 2006 after a review of 60 days - a notably fast clearance cycle.

This device falls under the Microbiology FDA review panel, regulated under 21 CFR 866.1640 - 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 Trek Diagnostic Systems, Inc. devices

Submission Details

510(k) Number K053243 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received November 21, 2005
Decision Date January 20, 2006
Days to Decision 60 days
Submission Type Traditional
Review Panel Microbiology (MI)
Summary Statement
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
42d faster than avg
Panel avg: 102d · This submission: 60d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code LRG Instrument For Auto Reader & Interpretation Of Overnight Suscept. Systems
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 866.1640
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 - LRG Instrument For Auto Reader & Interpretation Of Overnight Suscept. Systems

All 37
Devices cleared under the same product code (LRG) and FDA review panel - the closest regulatory comparables to K053243.
MICROSCAN MICROSTREP PLUS PANEL
K061872 · Dade Behring, Inc. · Aug 2006
MICROSCAN DRIED GRAM-POSITIVE MIC/COMBO PANELS WITH ERYTHROMYCIN (0.25 - 16UG/ML)
K062179 · Dade Behring, Inc. · Aug 2006
MICROSCAN MICROSTREP PLUS PANEL
K062276 · Dade Behring, Inc. · Aug 2006
MICROSCAN DRIED GRAM-POSITIVE MIC/COMBO PANELS WITH ERYTHROMYCIN
K050043 · Dade Behring, Inc. · Mar 2005
MICROSCAN DRIED GRAM NEGATIVE MIC/COMBO PANELS AMOXICILLIN/K. CLAVULANATE
K050585 · Dade Behring, Inc. · Mar 2005
MICROSCAN DRIED GRAM-POSITIVE MIC/COMBO PANELS WITH DAPTOMYCIN (0.03 - 16 MCG/ML)
K043545 · Dade Behring, Inc. · Feb 2005