Cleared Traditional

K812142 - LIC 180 MEDICAL LAMPS

K812142 is the FDA 510(k) clearance for LIC 180 MEDICAL LAMPS by Lada Intl., Inc.. It is a Class 1 General Hospital device (product code KZF) cleared through the Traditional 510(k) pathway after a 16-day FDA review.

K812142 · Lada Intl., Inc. · General Hospital
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Aug 1981
Decision
16d
Days
Class 1
Risk

K812142 is an FDA 510(k) clearance for the LIC 180 MEDICAL LAMPS. Classified as Device, Medical Examination, Ac Powered (product code KZF), Class I - General Controls.

Submitted by Lada Intl., Inc. (Mchenry, US). The FDA issued a Cleared decision on August 13, 1981 after a review of 16 days - a notably fast clearance cycle.

This device falls under the General Hospital FDA review panel, regulated under 21 CFR 880.6320 - the FDA general hospital 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 Lada Intl., Inc. devices

Submission Details

510(k) Number K812142 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 28, 1981
Decision Date August 13, 1981
Days to Decision 16 days
Submission Type Traditional
Review Panel General Hospital (HO)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
113d faster than avg
Panel avg: 129d · This submission: 16d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code KZF Device, Medical Examination, Ac Powered
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 880.6320
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 - KZF Device, Medical Examination, Ac Powered

All 8
Devices cleared under the same product code (KZF) and FDA review panel - the closest regulatory comparables to K812142.
EPISCOPE, MODEL 47300
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K800230 · Abco Dealers, Inc. · Feb 1980
HALOGEN EXAM. LITE #48400
K780628 · Welch Allyn, Inc. · Jun 1978