Cleared Traditional

K922392 - ITE

K922392 is an FDA 510(k) clearance for ITE, manufactured by A-1 Hearing Aid Lab. The device is a Class 1 Ear, Nose, Throat device with product code ESD cleared through the Traditional 510(k) pathway after a 51-day FDA review.

K922392 · A-1 Hearing Aid Lab · Ear, Nose, Throat device
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Jul 1992
Decision
51d
Days
Class 1
Risk

K922392 is an FDA 510(k) clearance for the ITE, ITC, OE(OPEN), HS(HALF SHELL) HEARING AID. Classified as Hearing Aid, Air-conduction, Prescription (product code ESD), Class I - General Controls.

Submitted by A-1 Hearing Aid Lab (Gulfport, US). The FDA issued a Cleared decision on July 10, 1992 after a review of 51 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 A-1 Hearing Aid Lab devices

FDA 510(k) Submission Details - K922392

510(k) Number K922392 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 20, 1992
Decision Date July 10, 1992
Days to Decision 51 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
38d faster than avg
Panel avg: 89d · This submission: 51d
Pathway characteristics
Predicate-based equivalence.

ESD Device Classification - Class 1, General Controls

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 K922392.
BTE HEARING AID OTICON MODEL: MULTIFOCUS POWER
K923388 · Oticon Corp. · Aug 1992
BTE HEARING AID PERSONIC 410
K923490 · Oticon Corp. · Aug 1992
BTE HEARING AID PERSONIC 425
K923491 · Oticon Corp. · Aug 1992
A-ZILICONE
K905555 · Oticon Corp. · Jul 1992
OTOSONIC ACS K
K922827 · Beltone Electronics Corp. · Jul 1992
WIDEX MODEL D32
K922708 · Widex Hearing Aid Co., Inc. · Jun 1992