Cleared Traditional

K993199 - POCKET CHAMBER VALVED AEROSOL HOLDING CHAMBER

K993199 is an FDA 510(k) clearance for POCKET CHAMBER VALVED AEROSOL HOLDING C..., manufactured by Ferraris Medical, Inc.. The device is a Class 2 Anesthesiology device with product code CAF cleared through the Traditional 510(k) pathway after a 187-day FDA review.

K993199 · Ferraris Medical, Inc. · Anesthesiology device
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Optimized for regulatory review, auditing and printing
Mar 2000
Decision
187d
Days
Class 2
Risk

K993199 is an FDA 510(k) clearance for the POCKET CHAMBER VALVED AEROSOL HOLDING CHAMBER. Classified as Nebulizer (direct Patient Interface) (product code CAF), Class II - Special Controls.

Submitted by Ferraris Medical, Inc. (Washington, US). The FDA issued a Cleared decision on March 28, 2000 after a review of 187 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 Ferraris Medical, Inc. devices

FDA 510(k) Submission Details - K993199

510(k) Number K993199 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 23, 1999
Decision Date March 28, 2000
Days to Decision 187 days
Submission Type Traditional
Review Panel Anesthesiology (AN)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
47d slower than avg
Panel avg: 140d · This submission: 187d
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 318
Devices cleared under the same product code (CAF) and FDA review panel - the closest regulatory comparables to K993199.
AERONEB II, MODEL APN 200
K992831 · Aerogen, Inc. · Aug 2000
BESTNEB PORTABLE AEROSOL THERAPY UNIT, AP-100100
K990435 · Apex Medical Corp. · Jun 2000
DEVILBISS NEBULIZER MODEL 800
K993492 · Sunrise Medical Hhg, Inc. · Apr 2000
SIDE DRAFT NEB-U-MIST NEBULIZER, MODEL 41896
K994352 · Hudson Respiratory Care, Inc. · Mar 2000
NELLCOR PURITAN BENNETT 700 SERIES VENTILATOR SYSTEM, AND EASYNEB NEBULIZER
K990897 · Puritan-Bennett Ireland, Ltd. · Mar 2000
METERED DOSE INHALER ADAPTER-DISPOSABLE, ADAPTER REUSABLE
K991355 · Instrumentation Industries, Inc. · Jan 2000