Cleared Traditional

K860845 - RESPIRONICS SECUREASY

K860845 is an FDA 510(k) clearance for RESPIRONICS SECUREASY, manufactured by Respironics, Inc.. The device is a Class 1 Anesthesiology device with product code CBH cleared through the Traditional 510(k) pathway after a 7-day FDA review.

K860845 · Respironics, Inc. · Anesthesiology device
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Mar 1986
Decision
7d
Days
Class 1
Risk

K860845 is an FDA 510(k) clearance for the RESPIRONICS SECUREASY. Classified as Device, Fixation, Tracheal Tube (product code CBH), Class I - General Controls.

Submitted by Respironics, Inc. (Monroeville, US). The FDA issued a Cleared decision on March 13, 1986 after a review of 7 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.

View all Respironics, Inc. devices

FDA 510(k) Submission Details - K860845

510(k) Number K860845 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 06, 1986
Decision Date March 13, 1986
Days to Decision 7 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
133d faster than avg
Panel avg: 140d · This submission: 7d
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 17
Devices cleared under the same product code (CBH) and FDA review panel - the closest regulatory comparables to K860845.
TRAKEFIT TRACHEOSTOMY TUBE HOLDER
K872277 · Ackrad Laboratories · Jul 1987
BABY E.T. TAPE(TM)
K871560 · B&B Medical Technologies, Inc. · May 1987
E. T. TAPE ENDOTRACHEAL TUBE HOLDER
K862084 · B&B Medical Technologies, Inc. · Jun 1986
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