Cleared Traditional

K233486 - 731 Series Ventilator

K233486 is the FDA 510(k) clearance for 731 Series Ventilator by ZOLL Medical Corporation. It is a Class 2 Anesthesiology device (product code CBK) cleared through the Traditional 510(k) pathway after a 413-day FDA review.

K233486 · ZOLL Medical Corporation · Anesthesiology device
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Dec 2024
Decision
413d
Days
Class 2
Risk

K233486 is an FDA 510(k) clearance for the 731 Series Ventilator. Classified as Ventilator, Continuous, Facility Use (product code CBK), Class II - Special Controls.

Submitted by ZOLL Medical Corporation (Chelsmford, US). The FDA issued a Cleared decision on December 13, 2024 after a review of 413 days - an unusually long review period, suggesting complex equivalence evaluation.

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: High-complexity regulatory submission. Elevated predicate reliance profile. The extended review timeline suggests the FDA required additional documentation before confirming substantial equivalence - a pattern common in complex or first-of-kind Anesthesiology submissions.

View all ZOLL Medical Corporation devices

Submission Details

510(k) Number K233486 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received October 27, 2023
Decision Date December 13, 2024
Days to Decision 413 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
273d slower than avg
Panel avg: 140d · This submission: 413d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

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 196
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