Cleared Traditional

K861989 - MODIFICATION OF SUNTANA SUN SYSTEM BED

K861989 is an FDA 510(k) clearance for MODIFICATION OF SUNTANA SUN SYSTEM BED, manufactured by Hawaiian Tan Spa. The device is a Class 2 General & Plastic Surgery device with product code FTC cleared through the Traditional 510(k) pathway after a 17-day FDA review.

K861989 · Hawaiian Tan Spa · General & Plastic Surgery device
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Jun 1986
Decision
17d
Days
Class 2
Risk

K861989 is an FDA 510(k) clearance for the MODIFICATION OF SUNTANA SUN SYSTEM BED. Classified as Light, Ultraviolet, Dermatological (product code FTC), Class II - Special Controls.

Submitted by Hawaiian Tan Spa (Huntsville, US). The FDA issued a Cleared decision on June 9, 1986 after a review of 17 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 Hawaiian Tan Spa devices

FDA 510(k) Submission Details - K861989

510(k) Number K861989 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 23, 1986
Decision Date June 09, 1986
Days to Decision 17 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
98d faster than avg
Panel avg: 115d · This submission: 17d
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 86
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