Cleared Traditional

K963681 - CCA-100 (MODIFIED)

K963681 is an FDA 510(k) clearance for CCA-100 (MODIFIED), manufactured by Benson Medical Instruments Co.. The device is a Class 2 Ear, Nose, Throat device with product code EWO cleared through the Traditional 510(k) pathway after a 89-day FDA review.

K963681 · Benson Medical Instruments Co. · Ear, Nose, Throat device
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Oct 1996
Decision
89d
Days
Class 2
Risk

K963681 is an FDA 510(k) clearance for the CCA-100 (MODIFIED). Classified as Audiometer (product code EWO), Class II - Special Controls.

Submitted by Benson Medical Instruments Co. (Minneapolis, US). The FDA issued a Cleared decision on October 8, 1996 after a review of 89 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 Benson Medical Instruments Co. devices

FDA 510(k) Submission Details - K963681

510(k) Number K963681 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 11, 1996
Decision Date October 08, 1996
Days to Decision 89 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
At panel average
Panel avg: 89d · This submission: 89d
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 64
Devices cleared under the same product code (EWO) and FDA review panel - the closest regulatory comparables to K963681.
MODIFICATION TO OTOACOUSTIC EMISSIONS (OAE0 TEST INSTRUMENT
K964132 · Bio-Logic Systems Corp. · May 1997
RACE CAR TYMPANOMETER WITH AUDIOMETER(AE-RCAUD I/QUIK TYMP 1(AE-QUIK 1)/QUICK TYMP 2(AE-QUIK 2)
K970279 · American Electromedics Corp. · Mar 1997
PORTAREM-3000, PFS-6000
K964340 · Starkey Laboratories, Inc. · Jan 1997
SCOUT SPORT - A MODIFICATION TO (FORMERLY EMAV) OTOACOUSTIC EMISSIONS (OAE) TEST INSTRUMENT
K961447 · Bio-Logic Systems Corp. · May 1996
PROPHET
K953884 · Qualitone · Oct 1995
BELTONE PERSONAL HEARING SCREENER
K943616 · Beltone Electronics Corp. · Jul 1995