Cleared Traditional

K882430 - HOOD TRACHEAL STOMA BUTTON

K882430 is an FDA 510(k) clearance for HOOD TRACHEAL STOMA BUTTON, manufactured by Hood Laboratories. The device is a Class 2 Anesthesiology device with product code BTO cleared through the Traditional 510(k) pathway after a 14-day FDA review.

K882430 · Hood Laboratories · Anesthesiology device
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Jun 1988
Decision
14d
Days
Class 2
Risk

K882430 is an FDA 510(k) clearance for the HOOD TRACHEAL STOMA BUTTON. Classified as Tube, Tracheostomy (w/wo Connector) (product code BTO), Class II - Special Controls.

Submitted by Hood Laboratories (Pembroke, US). The FDA issued a Cleared decision on June 28, 1988 after a review of 14 days - a notably fast clearance cycle.

This device falls under the Anesthesiology FDA review panel, regulated under 21 CFR 868.5800 - 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 Hood Laboratories devices

FDA 510(k) Submission Details - K882430

510(k) Number K882430 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 14, 1988
Decision Date June 28, 1988
Days to Decision 14 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
126d faster than avg
Panel avg: 140d · This submission: 14d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

BTO Device Classification - Class 2, Special Controls

Product Code BTO Tube, Tracheostomy (w/wo Connector)
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 868.5800
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 - BTO Tube, Tracheostomy (w/wo Connector)

All 58
Devices cleared under the same product code (BTO) and FDA review panel - the closest regulatory comparables to K882430.
HOOD PEDIATRIC TRACHEOSTOMY TUBE
K893866 · Hood Laboratories · Aug 1989
SHILEY PERC TRACHEOSTOMY SYSTEM
K884730 · Shiley, Inc. · Jan 1989
FOME-CUF TRACHEAL TUBES W/SIDEPORT AIRWAY CONNECT.
K884427 · Bivona Medical Technologies · Nov 1988
SHILEY DISP. CANNULA CUFFLESS TRACEOSTOMY TUBE
K880614 · Shiley, Inc. · Mar 1988
PREFILLED WATER FOR IRRIGATION USP
K880316 · Automatic Liquid Packaging, Inc. · Feb 1988
PREFILLED SODIUM CHLORIDE SOLUTION FOR IRRIGA. USP
K880317 · Automatic Liquid Packaging, Inc. · Feb 1988