Cleared Traditional

K882936 - ADJUSTABLE ENTRAINMENT NEBULIZER

K882936 is an FDA 510(k) clearance for ADJUSTABLE ENTRAINMENT NEBULIZER, manufactured by Automatic Liquid Packaging, Inc.. The device is a Class 2 Anesthesiology device with product code CAF cleared through the Traditional 510(k) pathway after a 180-day FDA review.

K882936 · Automatic Liquid Packaging, Inc. · Anesthesiology device
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Jan 1989
Decision
180d
Days
Class 2
Risk

K882936 is an FDA 510(k) clearance for the ADJUSTABLE ENTRAINMENT NEBULIZER. Classified as Nebulizer (direct Patient Interface) (product code CAF), Class II - Special Controls.

Submitted by Automatic Liquid Packaging, Inc. (Woodstock, US). The FDA issued a Cleared decision on January 9, 1989 after a review of 180 days - an extended review 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: 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 Automatic Liquid Packaging, Inc. devices

FDA 510(k) Submission Details - K882936

510(k) Number K882936 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 13, 1988
Decision Date January 09, 1989
Days to Decision 180 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
40d slower than avg
Panel avg: 140d · This submission: 180d
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 218
Devices cleared under the same product code (CAF) and FDA review panel - the closest regulatory comparables to K882936.
MEDIPART DISPOSABLE AEROSOL SYSTEM MP-070-PTD
K894138 · Medipart Jerry Alexander · Sep 1989
AEROCHAMBER M.V.
K884803 · Monaghan Medical Corp. · Apr 1989
HAND HELD NEBULIZER SYSTEM
K884947 · Salter Labs · Feb 1989
NEBULIZER HEATER
K882935 · Automatic Liquid Packaging, Inc. · Dec 1988
UNIT DOSE 3% SODIUM CHLORIDE SOLUTION FOR INHALA.
K884359 · Automatic Liquid Packaging, Inc. · Dec 1988
OMRON ULTRASONIC NEBULIZER NE-U06
K875134 · Nidek, Inc. · Dec 1988