Cleared Traditional

K070880 - ER35 ERO-SCAN PRO HEARING TEST SYSTEM

K070880 is an FDA 510(k) clearance for ER35 ERO-SCAN PRO HEARING TEST SYSTEM, manufactured by Etymotic Research, Inc.. The device is a Class 2 Ear, Nose, Throat device with product code EWO cleared through the Traditional 510(k) pathway after a 69-day FDA review.

K070880 · Etymotic Research, Inc. · Ear, Nose, Throat device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Jun 2007
Decision
69d
Days
Class 2
Risk

K070880 is an FDA 510(k) clearance for the ER35 ERO-SCAN PRO HEARING TEST SYSTEM. Classified as Audiometer (product code EWO), Class II - Special Controls.

Submitted by Etymotic Research, Inc. (Washington, US). The FDA issued a Cleared decision on June 7, 2007 after a review of 69 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 Etymotic Research, Inc. devices

FDA 510(k) Submission Details - K070880

510(k) Number K070880 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 30, 2007
Decision Date June 07, 2007
Days to Decision 69 days
Submission Type Traditional
Review Panel Ear, Nose, Throat (EN)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
20d faster than avg
Panel avg: 89d · This submission: 69d
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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