Cleared Traditional

K192324 - Sheridan Spiral-Flex Endotracheal Tubes

K192324 is the FDA 510(k) clearance for Sheridan Spiral-Flex Endotracheal Tubes by Teleflexmedical, Inc.. It is a Class 2 Anesthesiology device (product code BTR) cleared through the Traditional 510(k) pathway after a 101-day FDA review.

K192324 · Teleflexmedical, Inc. · Anesthesiology device
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Dec 2019
Decision
101d
Days
Class 2
Risk

K192324 is an FDA 510(k) clearance for the Sheridan Spiral-Flex Endotracheal Tubes. Classified as Tube, Tracheal (w/wo Connector) (product code BTR), Class II - Special Controls.

Submitted by Teleflexmedical, Inc. (Morrisville, US). The FDA issued a Cleared decision on December 6, 2019 after a review of 101 days - within the typical 510(k) review window.

This device falls under the Anesthesiology FDA review panel, regulated under 21 CFR 868.5730 - 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: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Anesthesiology review framework, consistent with the majority of Class II 510(k) submissions.

View all Teleflexmedical, Inc. devices

Submission Details

510(k) Number K192324 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 27, 2019
Decision Date December 06, 2019
Days to Decision 101 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
39d faster than avg
Panel avg: 140d · This submission: 101d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code BTR Tube, Tracheal (w/wo Connector)
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 868.5730
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 - BTR Tube, Tracheal (w/wo Connector)

All 107
Devices cleared under the same product code (BTR) and FDA review panel - the closest regulatory comparables to K192324.
Venner PneuX™ ETT (Endotracheal Tube) 6 mm, Venner PneuX™ ETT (Endotracheal Tube) 7 mm, Venner PneuX™ ETT (Endotracheal Tube) 8 mm, Venner PneuX™ ETT (Endotracheal Tube) 9 mm
K192120 · Venner Medical (Singapore) Pte, Ltd. · Feb 2020
Trach- Vac Endotracheal Tube (SFTVPU) Subglottic Suction Tube with Salter Flex-Tip and Salter ThinCuff, Trach- Vac Endotracheal Tube (SFTVVC) Subglottic Suction Tube with Salter Flex-Tip and Salter ThinCuff
K190878 · Salter Labs, Inc. · Jan 2020
Endotracheal Tube with Evacuation Lumen
K182739 · Well Lead Medical Co., Ltd. · Dec 2019
SolidAIRity III Airway Stabilization System
K190630 · Securisyn Medical, LLC · Oct 2019
Yikang Endotracheal Tube
K190213 · Jiangxi Yikang Medical Instrument Group Co., Ltd. · Sep 2019
Endotracheal Tube
K190274 · Tianjin Medis Medical Device Co., Ltd. · Jul 2019