Cleared Traditional

K822179 - FRENZEL EYEGLASSES & RELATED ITEMS

K822179 is the FDA 510(k) clearance for FRENZEL EYEGLASSES & RELATED ITEMS by Kelleher Corp.. It is a Class 1 Ear, Nose, Throat device (product code KHH) cleared through the Traditional 510(k) pathway after a 60-day FDA review.

K822179 · Kelleher Corp. · Ear, Nose, Throat device
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Sep 1982
Decision
60d
Days
Class 1
Risk

K822179 is an FDA 510(k) clearance for the FRENZEL EYEGLASSES & RELATED ITEMS. Classified as Stimulator, Caloric-air (product code KHH), Class I - General Controls.

Submitted by Kelleher Corp. (Mchenry, US). The FDA issued a Cleared decision on September 21, 1982 after a review of 60 days - a notably fast clearance cycle.

This device falls under the Ear, Nose, Throat FDA review panel, regulated under 21 CFR 874.1800 - 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 Kelleher Corp. devices

Submission Details

510(k) Number K822179 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 23, 1982
Decision Date September 21, 1982
Days to Decision 60 days
Submission Type Traditional
Review Panel Ear, Nose, Throat (EN)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
29d faster than avg
Panel avg: 89d · This submission: 60d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code KHH Stimulator, Caloric-air
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 874.1800
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.