Cleared Traditional

K792030 - TWO-PIECE I.P.P.B. MANIFOLD-WITH RIGHT

K792030 is an FDA 510(k) clearance for TWO-PIECE I.P.P.B. MANIFOLD-WITH RIGHT, manufactured by Airlife, Inc.. The device is a Class 1 Anesthesiology device with product code BZO cleared through the Traditional 510(k) pathway after a 21-day FDA review.

K792030 · Airlife, Inc. · Anesthesiology device
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Oct 1979
Decision
21d
Days
Class 1
Risk

K792030 is an FDA 510(k) clearance for the TWO-PIECE I.P.P.B. MANIFOLD-WITH RIGHT. Classified as Set, Tubing And Support, Ventilator (w Harness) (product code BZO), Class I - General Controls.

Submitted by Airlife, Inc. (Mchenry, US). The FDA issued a Cleared decision on October 30, 1979 after a review of 21 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 Airlife, Inc. devices

FDA 510(k) Submission Details - K792030

510(k) Number K792030 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received October 09, 1979
Decision Date October 30, 1979
Days to Decision 21 days
Submission Type Traditional
Review Panel Anesthesiology (AN)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
119d faster than avg
Panel avg: 140d · This submission: 21d
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 52
Devices cleared under the same product code (BZO) and FDA review panel - the closest regulatory comparables to K792030.
VENTILATOR CIRCUIT
K812774 · Hudson Oxygen Therapy Sales Co. · Oct 1981
CAM-10 RESPIRATORY HOSE ASSEMBLIES
K801859 · Lifecare Services, Inc. · Sep 1980
CIRCAPAK
K792268 · Respiratory Care, Inc. · Nov 1979
CIRCUIT, BREATHING (W/ CONNECTOR, ADAPT,
K792047 · Airlife, Inc. · Oct 1979
CIRCUIT, BREATHING W/WO NEBULIZER
K791761 · Airlife, Inc. · Oct 1979
Y & ELBOW W/WO PORTS
K791856 · Airlife, Inc. · Sep 1979