Cleared Traditional

K843046 - RELIANCE TREATMENT CABINET

K843046 is an FDA 510(k) clearance for RELIANCE TREATMENT CABINET, manufactured by F. & F. Koenigkramer. The device is a Class 1 Ear, Nose, Throat device with product code ETF cleared through the Traditional 510(k) pathway after a 56-day FDA review.

K843046 · F. & F. Koenigkramer · Ear, Nose, Throat device
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Sep 1984
Decision
56d
Days
Class 1
Risk

K843046 is an FDA 510(k) clearance for the RELIANCE TREATMENT CABINET. Classified as Unit, Examining/treatment, Ent (product code ETF), Class I - General Controls.

Submitted by F. & F. Koenigkramer (Mchenry, US). The FDA issued a Cleared decision on September 27, 1984 after a review of 56 days - a notably fast clearance cycle.

This device falls under the Ear, Nose, Throat FDA review panel, regulated under 21 CFR 874.5300 - 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 F. & F. Koenigkramer devices

FDA 510(k) Submission Details - K843046

510(k) Number K843046 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 02, 1984
Decision Date September 27, 1984
Days to Decision 56 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
34d faster than avg
Panel avg: 90d · This submission: 56d
Pathway characteristics
Predicate-based equivalence.

ETF Device Classification - Class 1, General Controls

Product Code ETF Unit, Examining/treatment, Ent
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 874.5300
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 - ETF Unit, Examining/treatment, Ent

All 25
Devices cleared under the same product code (ETF) and FDA review panel - the closest regulatory comparables to K843046.
JEDMED MAXIM ENT CABINET
K881958 · Jedmed Instrument Co. · Jul 1988
MICROMEDICS STERILE, DISPOSABLE ENT EXAM KIT
K860940 · Micromedics, Inc. · May 1986
LARYNGEAL MIRROR PRE-WARMER
K855021 · Jedmed Instrument Co. · Mar 1986
INSTRUMENT CABINET
K833882 · Jedmed Instrument Co. · Jan 1984
ENT TREATMENT UNITS
K822252 · Kelleher Corp. · Nov 1982
MULTIPLE, ENT CABINET #448
K822531 · Midmark Corp. · Sep 1982