Cleared Traditional

K152412 - T-32

Also marketed or referenced as:
T-40 T-44 T-52 T-72 TT-50

K152412 is the FDA 510(k) clearance for T-32 by Tanses Technologies, Inc.. It is a Class 2 General & Plastic Surgery device (product code LEJ) cleared through the Traditional 510(k) pathway after a 247-day FDA review.

K152412 · Tanses Technologies, Inc. · General & Plastic Surgery device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Apr 2016
Decision
247d
Days
Class 2
Risk

K152412 is an FDA 510(k) clearance for the T-32. Classified as Booth, Sun Tan (product code LEJ), Class II - Special Controls.

Submitted by Tanses Technologies, Inc. (Laval Quebec, CA). The FDA issued a Cleared decision on April 29, 2016 after a review of 247 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 Tanses Technologies, Inc. devices

Submission Details

510(k) Number K152412 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 26, 2015
Decision Date April 29, 2016
Days to Decision 247 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
132d slower than avg
Panel avg: 115d · This submission: 247d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

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.

Regulatory Peers - LEJ Booth, Sun Tan

All 12
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