Cleared Traditional

K933515 - BOOTY ENDOSCOPE WARMER

K933515 is an FDA 510(k) clearance for BOOTY ENDOSCOPE WARMER, manufactured by T-Med, Inc.. The device is a Class 2 General & Plastic Surgery device with product code GCI cleared through the Traditional 510(k) pathway after a 99-day FDA review.

K933515 · T-Med, Inc. · General & Plastic Surgery device
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Oct 1993
Decision
99d
Days
Class 2
Risk

K933515 is an FDA 510(k) clearance for the BOOTY ENDOSCOPE WARMER. Classified as Laryngoscope, Endoscope (product code GCI), Class II - Special Controls.

Submitted by T-Med, Inc. (Fort Worth, US). The FDA issued a Cleared decision on October 27, 1993 after a review of 99 days - within the typical 510(k) review window.

This device falls under the General & Plastic Surgery FDA review panel, regulated under 21 CFR 876.1500 - 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 T-Med, Inc. devices

FDA 510(k) Submission Details - K933515

510(k) Number K933515 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 20, 1993
Decision Date October 27, 1993
Days to Decision 99 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
16d faster than avg
Panel avg: 115d · This submission: 99d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

GCI Device Classification - Class 2, Special Controls

Product Code GCI Laryngoscope, Endoscope
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 876.1500
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 - GCI Laryngoscope, Endoscope

All 9
Devices cleared under the same product code (GCI) and FDA review panel - the closest regulatory comparables to K933515.
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