Cleared Traditional

K931661 - ULTRABRONZ SERIES 800 (ECLIPSE) TANNING BED

K931661 is an FDA 510(k) clearance for ULTRABRONZ SERIES 800 (ECLIPSE) TANNING BED, manufactured by Eurocut, Ltd.. The device is a Class 2 General & Plastic Surgery device with product code LEJ cleared through the Traditional 510(k) pathway after a 256-day FDA review.

K931661 · Eurocut, Ltd. · General & Plastic Surgery device
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Dec 1993
Decision
256d
Days
Class 2
Risk

K931661 is an FDA 510(k) clearance for the ULTRABRONZ SERIES 800 (ECLIPSE) TANNING BED. Classified as Booth, Sun Tan (product code LEJ), Class II - Special Controls.

Submitted by Eurocut, Ltd. (Agoura, US). The FDA issued a Cleared decision on December 17, 1993 after a review of 256 days - an extended review 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: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the General & Plastic Surgery review framework, consistent with the majority of Class II 510(k) submissions.

View all Eurocut, Ltd. devices

FDA 510(k) Submission Details - K931661

510(k) Number K931661 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 05, 1993
Decision Date December 17, 1993
Days to Decision 256 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary Statement
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
141d slower than avg
Panel avg: 115d · This submission: 256d
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.