Cleared Traditional

K092244 - MA61

K092244 is an FDA 510(k) clearance for MA61, manufactured by Diagnostic Group, LLC. The device is a Class 2 Ear, Nose, Throat device with product code EWO cleared through the Traditional 510(k) pathway after a 216-day FDA review.

K092244 · Diagnostic Group, LLC · Ear, Nose, Throat device
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Mar 2010
Decision
216d
Days
Class 2
Risk

K092244 is an FDA 510(k) clearance for the MA61, MA62, MA63 FAMILY OF PORTABLE AUDIOMETERS. Classified as Audiometer (product code EWO), Class II - Special Controls.

Submitted by Diagnostic Group, LLC (Minnesota, US). The FDA issued a Cleared decision on March 1, 2010 after a review of 216 days - an extended review cycle.

This device falls under the Ear, Nose, Throat FDA review panel, regulated under 21 CFR 874.1050 - the FDA ear, nose and throat 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: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Ear, Nose, Throat review framework, consistent with the majority of Class II 510(k) submissions.

View all Diagnostic Group, LLC devices

FDA 510(k) Submission Details - K092244

510(k) Number K092244 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 28, 2009
Decision Date March 01, 2010
Days to Decision 216 days
Submission Type Traditional
Review Panel Ear, Nose, Throat (EN)
Summary Statement
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
127d slower than avg
Panel avg: 89d · This submission: 216d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

EWO Device Classification - Class 2, Special Controls

Product Code EWO Audiometer
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 874.1050
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 Ear, Nose, Throat devices follow this clearance model.

Regulatory Peers - EWO Audiometer

All 55
Devices cleared under the same product code (EWO) and FDA review panel - the closest regulatory comparables to K092244.
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