Cleared Traditional

K926055 - THE MILLER NEBULIZER SYSTEM

K926055 is an FDA 510(k) clearance for THE MILLER NEBULIZER SYSTEM, manufactured by Warren C. Miller. The device is a Class 2 Anesthesiology device with product code CAF cleared through the Traditional 510(k) pathway after a 90-day FDA review.

K926055 · Warren C. Miller · Anesthesiology device
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Feb 1993
Decision
90d
Days
Class 2
Risk

K926055 is an FDA 510(k) clearance for the THE MILLER NEBULIZER SYSTEM. Classified as Nebulizer (direct Patient Interface) (product code CAF), Class II - Special Controls.

Submitted by Warren C. Miller (Houston, US). The FDA issued a Cleared decision on February 3, 1993 after a review of 90 days - within the typical 510(k) review window.

This device falls under the Anesthesiology FDA review panel, regulated under 21 CFR 868.5630 - the FDA anesthesiology and respiratory 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: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Anesthesiology review framework, consistent with the majority of Class II 510(k) submissions.

View all Warren C. Miller devices

FDA 510(k) Submission Details - K926055

510(k) Number K926055 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received November 05, 1992
Decision Date February 03, 1993
Days to Decision 90 days
Submission Type Traditional
Review Panel Anesthesiology (AN)
Summary Statement
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
50d faster than avg
Panel avg: 140d · This submission: 90d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

CAF Device Classification - Class 2, Special Controls

Product Code CAF Nebulizer (direct Patient Interface)
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 868.5630
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 Anesthesiology devices follow this clearance model.

Regulatory Peers - CAF Nebulizer (direct Patient Interface)

All 438
Devices cleared under the same product code (CAF) and FDA review panel - the closest regulatory comparables to K926055.
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BETAMIST 2
K923698 · Rantran, Inc. · Feb 1993
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MICROFLOW
K924684 · Mountain Medical Equipment, Inc. · Dec 1992
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K921809 · Puritan Bennett Corp. · Dec 1992