Cleared Traditional

K940313 - PHONIC EAR

K940313 is the FDA 510(k) clearance for PHONIC EAR by Phonic Ear, Inc.. It is a Class 2 Ear, Nose, Throat device (product code EPF) cleared through the Traditional 510(k) pathway after a 57-day FDA review.

K940313 · Phonic Ear, Inc. · Ear, Nose, Throat device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Mar 1994
Decision
57d
Days
Class 2
Risk

K940313 is an FDA 510(k) clearance for the PHONIC EAR. Classified as Hearing Aid, Group And Auditory Trainer (product code EPF), Class II - Special Controls.

Submitted by Phonic Ear, Inc. (Petaluma, US). The FDA issued a Cleared decision on March 22, 1994 after a review of 57 days - a notably fast clearance cycle.

This device falls under the Ear, Nose, Throat FDA review panel, regulated under 21 CFR 874.3320 - 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 Phonic Ear, Inc. devices

Submission Details

510(k) Number K940313 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 24, 1994
Decision Date March 22, 1994
Days to Decision 57 days
Submission Type Traditional
Review Panel Ear, Nose, Throat (EN)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
32d faster than avg
Panel avg: 89d · This submission: 57d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code EPF Hearing Aid, Group And Auditory Trainer
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 874.3320
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 - EPF Hearing Aid, Group And Auditory Trainer

All 20
Devices cleared under the same product code (EPF) and FDA review panel - the closest regulatory comparables to K940313.
FM RECEIVER - AUDITORY TRAINER
K974287 · Phonic Ear, Inc. · Feb 1998
GROUP AUDITORY TRAINER (GROUP AMPLIFICATION SYSTEM)
K950730 · Phonic Ear, Inc. · Jun 1995
PHONAK MICROVOX RESONAL FM SYSTEM
K941768 · Phonak, Inc. · Jun 1994
PE 400IR, PE 400T, PE 400E
K923234 · Phonic Ear, Inc. · Sep 1992
GROUP AUDITORY TRAINING SYSTEM
K922720 · Phonic Ear, Inc. · Aug 1992
RESOUND PERSONAL HEARING SYSTEM SOUNDLINK-1
K922570 · Resound Corp. · Aug 1992