Cleared Traditional

K945314 - CLEVELAND TUBING, INC. EXPANDABLE/COLLAPSIBLEMEDICAL TUBING (FDA 510(k) Clearance)

Class I Anesthesiology device.

K945314 · Cleveland Tubing, Inc. · Anesthesiology device
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Nov 1994
Decision
17d
Days
Class 1
Risk

K945314 is an FDA 510(k) clearance for the CLEVELAND TUBING, INC. EXPANDABLE/COLLAPSIBLEMEDICAL TUBING. Classified as Circuit, Breathing (w Connector, Adaptor, Y Piece) (product code CAI), Class I - General Controls.

Submitted by Cleveland Tubing, Inc. (Cleveland, US). The FDA issued a Cleared decision on November 18, 1994 after a review of 17 days - a notably fast clearance 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: 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 Cleveland Tubing, Inc. devices

Submission Details

510(k) Number K945314 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received November 01, 1994
Decision Date November 18, 1994
Days to Decision 17 days
Submission Type Traditional
Review Panel Anesthesiology (AN)
Summary Statement
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
122d faster than avg
Panel avg: 139d · This submission: 17d
Pathway characteristics
Predicate-based equivalence.

Device Classification

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.