Cleared Traditional

K951147 - LEIGH MED. TECH. LARYNGOSCOPE BLADE COVER

K951147 is the FDA 510(k) clearance for LEIGH MED. TECH. LARYNGOSCOPE BLADE COVER by Leigh Med Tech, Inc.. It is a Class 1 Anesthesiology device (product code CCW) cleared through the Traditional 510(k) pathway after a 87-day FDA review.

K951147 · Leigh Med Tech, Inc. · Anesthesiology device
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Jun 1995
Decision
87d
Days
Class 1
Risk

K951147 is an FDA 510(k) clearance for the LEIGH MED. TECH. LARYNGOSCOPE BLADE COVER. Classified as Laryngoscope, Rigid (product code CCW), Class I - General Controls.

Submitted by Leigh Med Tech, Inc. (Maryland Heights, US). The FDA issued a Cleared decision on June 8, 1995 after a review of 87 days - a notably fast clearance cycle.

This device falls under the Anesthesiology FDA review panel, regulated under 21 CFR 868.5540 - 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 Leigh Med Tech, Inc. devices

Submission Details

510(k) Number K951147 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 13, 1995
Decision Date June 08, 1995
Days to Decision 87 days
Submission Type Traditional
Review Panel Anesthesiology (AN)
Summary Statement
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
53d faster than avg
Panel avg: 140d · This submission: 87d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code CCW Laryngoscope, Rigid
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 868.5540
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 - CCW Laryngoscope, Rigid

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