Cleared Traditional

K063338 - HEARID+TE TRANSIENT-EVOKED OTOACOUSTIC ...

K063338 is an FDA 510(k) clearance for HEARID+TE TRANSIENT-EVOKED OTOACOUSTIC ..., manufactured by Mimosa Acoustics, Inc.. The device is a Class 2 Ear, Nose, Throat device with product code EWO cleared through the Traditional 510(k) pathway after a 59-day FDA review.

K063338 · Mimosa Acoustics, Inc. · Ear, Nose, Throat device
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Jan 2007
Decision
59d
Days
Class 2
Risk

K063338 is an FDA 510(k) clearance for the HEARID+TE TRANSIENT-EVOKED OTOACOUSTIC EMISSIONS ANALYZER. Classified as Audiometer (product code EWO), Class II - Special Controls.

Submitted by Mimosa Acoustics, Inc. (Champaign, US). The FDA issued a Cleared decision on January 4, 2007 after a review of 59 days - a notably fast clearance 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: 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 Mimosa Acoustics, Inc. devices

FDA 510(k) Submission Details - K063338

510(k) Number K063338 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received November 06, 2006
Decision Date January 04, 2007
Days to Decision 59 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
30d faster than avg
Panel avg: 89d · This submission: 59d
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
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