Cleared Traditional

K901714 - LIFESTYLE HOME TANNING UNITS

K901714 is an FDA 510(k) clearance for LIFESTYLE HOME TANNING UNITS, manufactured by Life Products, Inc.. The device is a Class 2 General & Plastic Surgery device with product code LEJ cleared through the Traditional 510(k) pathway after a 75-day FDA review.

K901714 · Life Products, Inc. · General & Plastic Surgery device
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Jun 1990
Decision
75d
Days
Class 2
Risk

K901714 is an FDA 510(k) clearance for the LIFESTYLE HOME TANNING UNITS. Classified as Booth, Sun Tan (product code LEJ), Class II - Special Controls.

Submitted by Life Products, Inc. (Atlanta, US). The FDA issued a Cleared decision on June 27, 1990 after a review of 75 days - a notably fast clearance cycle.

This device falls under the General & Plastic Surgery FDA review panel, regulated under 21 CFR 878.4635 - 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 Life Products, Inc. devices

FDA 510(k) Submission Details - K901714

510(k) Number K901714 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 13, 1990
Decision Date June 27, 1990
Days to Decision 75 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
40d faster than avg
Panel avg: 115d · This submission: 75d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

LEJ Device Classification - Class 2, Special Controls

Product Code LEJ Booth, Sun Tan
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 878.4635
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.