Cleared Traditional

K810737 - ENDOTRACHEAL TUBE HOLDER

K810737 is an FDA 510(k) clearance for ENDOTRACHEAL TUBE HOLDER, manufactured by Aircare Systems. The device is a Class 1 Anesthesiology device with product code CBH cleared through the Traditional 510(k) pathway after a 30-day FDA review.

K810737 · Aircare Systems · Anesthesiology device
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Apr 1981
Decision
30d
Days
Class 1
Risk

K810737 is an FDA 510(k) clearance for the ENDOTRACHEAL TUBE HOLDER. Classified as Device, Fixation, Tracheal Tube (product code CBH), Class I - General Controls.

Submitted by Aircare Systems (Mchenry, US). The FDA issued a Cleared decision on April 17, 1981 after a review of 30 days - a notably fast clearance cycle.

This device falls under the Anesthesiology FDA review panel, regulated under 21 CFR 868.5770 - 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.

FDA 510(k) Submission Details - K810737

510(k) Number K810737 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 18, 1981
Decision Date April 17, 1981
Days to Decision 30 days
Submission Type Traditional
Review Panel Anesthesiology (AN)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
110d faster than avg
Panel avg: 140d · This submission: 30d
Pathway characteristics
Predicate-based equivalence.

CBH Device Classification - Class 1, General Controls

Product Code CBH Device, Fixation, Tracheal Tube
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 868.5770
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 - CBH Device, Fixation, Tracheal Tube

All 38
Devices cleared under the same product code (CBH) and FDA review panel - the closest regulatory comparables to K810737.
OR TUBE RESTRAINT
K851874 · Kinetic Concepts, Inc. · Aug 1985
RESPIRONICS ENDO TUBE CONTROL SYS
K822794 · Respironics, Inc. · Oct 1982
N-D0-SURE
K811185 · Ackrad Laboratories · Jun 1981
ENDOTRACHEAL TUBE HOLDER
K802601 · Hudson Oxygen Therapy Sales Co. · Dec 1980
LUBE-LOK
K781695 · Olympic Medical Corp. · Nov 1978
K810737 · ENDOTRACHEAL TUBE HOLDER
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