Cleared Traditional

K792218 - MISTY BEBULIZER

K792218 is an FDA 510(k) clearance for MISTY BEBULIZER, manufactured by Airlife, Inc.. The device is a Class 2 Anesthesiology device with product code CAF cleared through the Traditional 510(k) pathway after a 22-day FDA review.

K792218 · Airlife, Inc. · Anesthesiology device
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Nov 1979
Decision
22d
Days
Class 2
Risk

K792218 is an FDA 510(k) clearance for the MISTY BEBULIZER. Classified as Nebulizer (direct Patient Interface) (product code CAF), Class II - Special Controls.

Submitted by Airlife, Inc. (Mchenry, US). The FDA issued a Cleared decision on November 27, 1979 after a review of 22 days - a notably fast clearance cycle.

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: 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 Airlife, Inc. devices

FDA 510(k) Submission Details - K792218

510(k) Number K792218 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received November 05, 1979
Decision Date November 27, 1979
Days to Decision 22 days
Submission Type Traditional
Review Panel Anesthesiology (AN)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
118d faster than avg
Panel avg: 140d · This submission: 22d
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 229
Devices cleared under the same product code (CAF) and FDA review panel - the closest regulatory comparables to K792218.
0.9% SODIUM CHLORIDE SOL./RESP. THERAPY
K800295 · Abbott Laboratories · Mar 1980
NEBULIZER TUBING SET
K800083 · Abbott Laboratories · Jan 1980
TEE ADAPTER
K792364 · Airlife, Inc. · Dec 1979
I.P.P.B. MANIFOLDS & NEB. SING. & DBL
K791820 · Airlife, Inc. · Sep 1979
DISPOSABLE MEDICATION NEBULIZER
K791536 · Hospitak, Inc. · Sep 1979
TWO-PIECE IPPB MANIFOLD FOR SUPPLY LINE
K791443 · Airlife, Inc. · Aug 1979