Cleared Traditional

K833055 - LARYNGOSCOPE BLADES/HANDLES & LAMPS

K833055 is an FDA 510(k) clearance for LARYNGOSCOPE BLADES/HANDLES & LAMPS, manufactured by Medovations, Inc.. The device is a Class 1 Anesthesiology device with product code CCW cleared through the Traditional 510(k) pathway after a 68-day FDA review.

K833055 · Medovations, Inc. · Anesthesiology device
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Nov 1983
Decision
68d
Days
Class 1
Risk

K833055 is an FDA 510(k) clearance for the LARYNGOSCOPE BLADES/HANDLES & LAMPS. Classified as Laryngoscope, Rigid (product code CCW), Class I - General Controls.

Submitted by Medovations, Inc. (Walker, US). The FDA issued a Cleared decision on November 14, 1983 after a review of 68 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 Medovations, Inc. devices

FDA 510(k) Submission Details - K833055

510(k) Number K833055 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 07, 1983
Decision Date November 14, 1983
Days to Decision 68 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
72d faster than avg
Panel avg: 140d · This submission: 68d
Pathway characteristics
Predicate-based equivalence.

CCW Device Classification - Class 1, General Controls

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

All 28
Devices cleared under the same product code (CCW) and FDA review panel - the closest regulatory comparables to K833055.
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AUGUSTINE INTUBATION GUIDE(TM)
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K830047 · Welch Allyn, Inc. · Jan 1983
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