Cleared Traditional

K132021 - AHP 300, EMERGENCY PORTABLE VENTILATOR

K132021 is an FDA 510(k) clearance for AHP 300, manufactured by Allied Healthcare Products, Inc.. The device is a Class 2 Anesthesiology device with product code BTL cleared through the Traditional 510(k) pathway after a 274-day FDA review.

K132021 · Allied Healthcare Products, Inc. · Anesthesiology device
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Apr 2014
Decision
274d
Days
Class 2
Risk

K132021 is an FDA 510(k) clearance for the AHP 300, EMERGENCY PORTABLE VENTILATOR. Classified as Ventilator, Emergency, Powered (resuscitator) (product code BTL), Class II - Special Controls.

Submitted by Allied Healthcare Products, Inc. (Saint Louis, US). The FDA issued a Cleared decision on April 2, 2014 after a review of 274 days - an extended review cycle.

This device falls under the Anesthesiology FDA review panel, regulated under 21 CFR 868.5925 - 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 Allied Healthcare Products, Inc. devices

FDA 510(k) Submission Details - K132021

510(k) Number K132021 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 02, 2013
Decision Date April 02, 2014
Days to Decision 274 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
134d slower than avg
Panel avg: 140d · This submission: 274d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

BTL Device Classification - Class 2, Special Controls

Product Code BTL Ventilator, Emergency, Powered (resuscitator)
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 868.5925
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 - BTL Ventilator, Emergency, Powered (resuscitator)

All 78
Devices cleared under the same product code (BTL) and FDA review panel - the closest regulatory comparables to K132021.
MOVES SLC
K140049 · Thornhill Research, Inc. · May 2014
LIFEBORNE INFANT RESUSCITATOR
K140707 · International Biomedical · May 2014
EMERGENCY PORTABLE VENTILATOR
K131098 · Allied Healthcare Products, Inc. · Apr 2014
VENTRAIN
K132759 · Dolphys Medical B.V. · Mar 2014
SAVE II, SAVE II BASIC
K131877 · Automedx, Inc. · Mar 2014
PNEUPAC PARAPAC PLUS
K123957 · Smiths Medical International , Ltd. · Sep 2013