Cleared Traditional

K911154 - SUN MEDICAL SMOKE/FLUID EVAC SYST

K911154 is the FDA 510(k) clearance for SUN MEDICAL SMOKE/FLUID EVAC SYST by Sun Medical, Inc.. It is a Class 2 General Hospital device (product code FYD) cleared through the Traditional 510(k) pathway after a 133-day FDA review.

K911154 · Sun Medical, Inc. · General Hospital
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Jul 1991
Decision
133d
Days
Class 2
Risk

K911154 is an FDA 510(k) clearance for the SUN MEDICAL SMOKE/FLUID EVAC SYST, MODEL SFE-200. Classified as Apparatus, Exhaust, Surgical (product code FYD), Class II - Special Controls.

Submitted by Sun Medical, Inc. (Arlington, US). The FDA issued a Cleared decision on July 26, 1991 after a review of 133 days - within the typical 510(k) review window.

This device falls under the General Hospital FDA review panel, regulated under 21 CFR 878.5070 - the FDA general hospital 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 Hospital review framework, consistent with the majority of Class II 510(k) submissions.

View all Sun Medical, Inc. devices

Submission Details

510(k) Number K911154 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 15, 1991
Decision Date July 26, 1991
Days to Decision 133 days
Submission Type Traditional
Review Panel General Hospital (HO)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
4d slower than avg
Panel avg: 129d · This submission: 133d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code FYD Apparatus, Exhaust, Surgical
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 878.5070
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 Hospital devices follow this clearance model.