Cleared Traditional

K952929 - LD GENERAL PURPOSE DISINFECTANT

K952929 is the FDA 510(k) clearance for LD GENERAL PURPOSE DISINFECTANT by Alcide Corp.. It is a Class 1 General Hospital device (product code LRJ) cleared through the Traditional 510(k) pathway after a 110-day FDA review.

K952929 · Alcide Corp. · General Hospital
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Oct 1995
Decision
110d
Days
Class 1
Risk

K952929 is an FDA 510(k) clearance for the LD GENERAL PURPOSE DISINFECTANT. Classified as Disinfectant, Medical Devices (product code LRJ), Class I - General Controls.

Submitted by Alcide Corp. (Redmond, US). The FDA issued a Cleared decision on October 7, 1995 after a review of 110 days - within the typical 510(k) review window.

This device falls under the General Hospital FDA review panel, regulated under 21 CFR 880.6890 - 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: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the General Hospital review framework, consistent with the majority of Class II 510(k) submissions.

View all Alcide Corp. devices

Submission Details

510(k) Number K952929 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 19, 1995
Decision Date October 07, 1995
Days to Decision 110 days
Submission Type Traditional
Review Panel General Hospital (HO)
Summary Statement
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
19d faster than avg
Panel avg: 129d · This submission: 110d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code LRJ Disinfectant, Medical Devices
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 880.6890
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 - LRJ Disinfectant, Medical Devices

All 12
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