Cleared Traditional

ACUTEK'S CLEARPASSAGE (K951644) - FDA 510(k) Clearance

Class I Ear, Nose, Throat device.

K951644 · Acutek Adhesive Specialties, Inc. · Ear, Nose, Throat device
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Jul 1995
Decision
84d
Days
Class 1
Risk

K951644 is an FDA 510(k) clearance for the ACUTEK'S CLEARPASSAGE. Classified as Dilator, Nasal (product code LWF), Class I - General Controls.

Submitted by Acutek Adhesive Specialties, Inc. (Inglewood, US). The FDA issued a Cleared decision on July 3, 1995 after a review of 84 days - a notably fast clearance cycle.

This device falls under the Ear, Nose, Throat FDA review panel, regulated under 21 CFR 874.3900 - the FDA ear, nose and throat 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 Acutek Adhesive Specialties, Inc. devices

Submission Details

510(k) Number K951644 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 10, 1995
Decision Date July 03, 1995
Days to Decision 84 days
Submission Type Traditional
Review Panel Ear, Nose, Throat (EN)
Summary Statement
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
5d faster than avg
Panel avg: 89d · This submission: 84d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code LWF Dilator, Nasal
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 874.3900
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.