Cleared Traditional

K820248 - RODDER VOLUME VENTILATOR

K820248 is an FDA 510(k) clearance for RODDER VOLUME VENTILATOR, manufactured by Pharmaquest Corp.. The device is a Class 2 Anesthesiology device with product code CBK cleared through the Traditional 510(k) pathway after a 77-day FDA review.

K820248 · Pharmaquest Corp. · Anesthesiology device
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Apr 1982
Decision
77d
Days
Class 2
Risk

K820248 is an FDA 510(k) clearance for the RODDER VOLUME VENTILATOR. Classified as Ventilator, Continuous, Facility Use (product code CBK), Class II - Special Controls.

Submitted by Pharmaquest Corp. (Mchenry, US). The FDA issued a Cleared decision on April 16, 1982 after a review of 77 days - a notably fast clearance cycle.

This device falls under the Anesthesiology FDA review panel, regulated under 21 CFR 868.5895 - 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 Pharmaquest Corp. devices

FDA 510(k) Submission Details - K820248

510(k) Number K820248 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 29, 1982
Decision Date April 16, 1982
Days to Decision 77 days
Submission Type Traditional
Review Panel Anesthesiology (AN)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
63d faster than avg
Panel avg: 140d · This submission: 77d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

CBK Device Classification - Class 2, Special Controls

Product Code CBK Ventilator, Continuous, Facility Use
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 868.5895
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 - CBK Ventilator, Continuous, Facility Use

All 397
Devices cleared under the same product code (CBK) and FDA review panel - the closest regulatory comparables to K820248.
ABT 4000 VENTILATOR
K822233 · Kontron Instruments, Inc. · Aug 1982
SECHRIST MODEL 990 JET VENTILATOR
K821930 · Sechrist Industries, Inc. · Aug 1982
OHIO 7000 ELECTRONIC ANESTHESIA VENTIL.
K821376 · Ohio Medical Products · Jun 1982
NEWPORT VENTILATOR MODEL E100
K820746 · Newport Medical Instruments, Inc. · Apr 1982
ANESTHESIA VENTILATOR
K820393 · Puritan Bennett Corp. · Mar 1982
VENTILATOR MODELS
K820220 · Pneupac , Ltd. · Feb 1982