Cleared Traditional

K932119 - CLEVELAND TUBING, INC. VENTILATOR HOSES

K932119 is an FDA 510(k) clearance for CLEVELAND TUBING, manufactured by Cleveland Tubing, Inc.. The device is a Class 1 Anesthesiology device with product code BZO cleared through the Traditional 510(k) pathway after a 51-day FDA review.

K932119 · Cleveland Tubing, Inc. · Anesthesiology device
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Jun 1993
Decision
51d
Days
Class 1
Risk

K932119 is an FDA 510(k) clearance for the CLEVELAND TUBING, INC. VENTILATOR HOSES. Classified as Set, Tubing And Support, Ventilator (w Harness) (product code BZO), Class I - General Controls.

Submitted by Cleveland Tubing, Inc. (Cleveland, US). The FDA issued a Cleared decision on June 23, 1993 after a review of 51 days - a notably fast clearance cycle.

This device falls under the Anesthesiology FDA review panel, regulated under 21 CFR 868.5975 - 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

FDA 510(k) Submission Details - K932119

510(k) Number K932119 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 03, 1993
Decision Date June 23, 1993
Days to Decision 51 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
89d faster than avg
Panel avg: 140d · This submission: 51d
Pathway characteristics
Predicate-based equivalence.

BZO Device Classification - Class 1, General Controls

Product Code BZO Set, Tubing And Support, Ventilator (w Harness)
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 868.5975
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 - BZO Set, Tubing And Support, Ventilator (w Harness)

All 53
Devices cleared under the same product code (BZO) and FDA review panel - the closest regulatory comparables to K932119.
VOLUME VENTILATORS
K932560 · Life Shield Healthcare Products, Inc. · Jul 1993
PRECISION MED PRODUCTS LTD VOLUME VENTILATORS
K932712 · Precision Med Products, Ltd. · Jul 1993
VENTILATOR HOSES
K932563 · Life Shield Healthcare Products, Inc. · Jul 1993
DISPOSABLE ANESTHESIA BREATHING CIRCUIT, MODIFIED
K922479 · Intertech Resources, Inc. · Oct 1992
GAS SAMPLING KIT MODIFICATION
K921510 · Respiratory Support Products, Inc. · Jun 1992
UNIVERSAL VOLUME VENTILATOR CIRCUIT, MODIFICATION
K911328 · Intertech Resources, Inc. · Aug 1991