Cleared Traditional

K844039 - AZTECH INDUSTRIES SUNTANNING BED AZ100

K844039 is an FDA 510(k) clearance for AZTECH INDUSTRIES SUNTANNING BED AZ100, manufactured by Aztech Industries, Inc.. The device is a Class 2 General & Plastic Surgery device with product code FTC cleared through the Traditional 510(k) pathway after a 20-day FDA review.

K844039 · Aztech Industries, Inc. · General & Plastic Surgery device
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Nov 1984
Decision
20d
Days
Class 2
Risk

K844039 is an FDA 510(k) clearance for the AZTECH INDUSTRIES SUNTANNING BED AZ100. Classified as Light, Ultraviolet, Dermatological (product code FTC), Class II - Special Controls.

Submitted by Aztech Industries, Inc. (Portland, US). The FDA issued a Cleared decision on November 5, 1984 after a review of 20 days - a notably fast clearance cycle.

This device falls under the General & Plastic Surgery FDA review panel, regulated under 21 CFR 878.4630 - the FDA general and plastic surgery 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 Aztech Industries, Inc. devices

FDA 510(k) Submission Details - K844039

510(k) Number K844039 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received October 16, 1984
Decision Date November 05, 1984
Days to Decision 20 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
95d faster than avg
Panel avg: 115d · This submission: 20d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

FTC Device Classification - Class 2, Special Controls

Product Code FTC Light, Ultraviolet, Dermatological
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 878.4630
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most General & Plastic Surgery devices follow this clearance model.

Regulatory Peers - FTC Light, Ultraviolet, Dermatological

All 88
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