Cleared Traditional

K782053 - HEARING AID

K782053 is the FDA 510(k) clearance for HEARING AID by Hc Electronics. It is a Class 1 Ear, Nose, Throat device (product code ESD) cleared through the Traditional 510(k) pathway after a 8-day FDA review.

K782053 · Hc Electronics · Ear, Nose, Throat device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Dec 1978
Decision
8d
Days
Class 1
Risk

K782053 is an FDA 510(k) clearance for the HEARING AID, POST-AURICULAR. Classified as Hearing Aid, Air-conduction, Prescription (product code ESD), Class I - General Controls.

Submitted by Hc Electronics (Mchenry, US). The FDA issued a Cleared decision on December 15, 1978 after a review of 8 days - a notably fast clearance cycle.

This device falls under the Ear, Nose, Throat FDA review panel, regulated under 21 CFR 874.3300 - 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 Hc Electronics devices

Submission Details

510(k) Number K782053 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 07, 1978
Decision Date December 15, 1978
Days to Decision 8 days
Submission Type Traditional
Review Panel Ear, Nose, Throat (EN)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
81d faster than avg
Panel avg: 89d · This submission: 8d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code ESD Hearing Aid, Air-conduction, Prescription
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 874.3300
Definition An Air-conduction Hearing Aid Is A Wearable Sound Amplifying Device Intended To Compensate For Impaired Hearing That Conducts Sound To The Ear Through The Air. This Is A Prescription Hearing Aid.
What this classification means

Class I devices are subject to general controls only and most are exempt from 510(k) premarket notification. They represent the lowest regulatory burden in the FDA device framework.

Regulatory Peers - ESD Hearing Aid, Air-conduction, Prescription

All 740
Devices cleared under the same product code (ESD) and FDA review panel - the closest regulatory comparables to K782053.
MODULE PERSONAL EAR (DELUXE)
K790095 · Qualitone · Jan 1979
HEARING AID, MODEL GB
K782121 · Dahlberg Electronics, Inc. · Jan 1979
HEARING AID, MODEL AA
K782122 · Dahlberg Electronics, Inc. · Jan 1979
HEARING AID, ITE MODULAR MODEL I, II, V
K781663 · Oticon Corp. · Oct 1978
HEARING AID, UNITRON MODEL 960PL
K781513 · Unitron Industries, Inc. · Sep 1978
HEARING AID, UNITRON MODEL 761P
K781502 · Unitron Industries, Inc. · Sep 1978