Cleared Traditional

K932781 - DUAL VALVED RESPIRATORY T

K932781 is an FDA 510(k) clearance for DUAL VALVED RESPIRATORY T, manufactured by Innovations For Mechanical Ventilation, Inc.. The device is a Class 1 Anesthesiology device with product code CAI cleared through the Traditional 510(k) pathway after a 229-day FDA review.

K932781 · Innovations For Mechanical Ventilation, Inc. · Anesthesiology device
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Jan 1994
Decision
229d
Days
Class 1
Risk

K932781 is an FDA 510(k) clearance for the DUAL VALVED RESPIRATORY T. Classified as Circuit, Breathing (w Connector, Adaptor, Y Piece) (product code CAI), Class I - General Controls.

Submitted by Innovations For Mechanical Ventilation, Inc. (New City, US). The FDA issued a Cleared decision on January 24, 1994 after a review of 229 days - an extended review cycle.

This device falls under the Anesthesiology FDA review panel, regulated under 21 CFR 868.5240 - 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 Innovations For Mechanical Ventilation, Inc. devices

FDA 510(k) Submission Details - K932781

510(k) Number K932781 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 09, 1993
Decision Date January 24, 1994
Days to Decision 229 days
Submission Type Traditional
Review Panel Anesthesiology (AN)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
89d slower than avg
Panel avg: 140d · This submission: 229d
Pathway characteristics
Predicate-based equivalence.

CAI Device Classification - Class 1, General Controls

Product Code CAI Circuit, Breathing (w Connector, Adaptor, Y Piece)
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 868.5240
What this classification means

Class I devices are subject to general controls only and most are exempt from 510(k) premarket notification. They represent the lowest regulatory burden in the FDA device framework.

Regulatory Peers - CAI Circuit, Breathing (w Connector, Adaptor, Y Piece)

All 123
Devices cleared under the same product code (CAI) and FDA review panel - the closest regulatory comparables to K932781.
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THE INFANT FLOW SYSTEM
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K932562 · Life Shield Healthcare Products, Inc. · Jul 1993