Cleared Abbreviated

K080796 - SRI LP DRAPE

K080796 is an FDA 510(k) clearance for SRI LP DRAPE, manufactured by Sri/Surgical Express. The device is a Class 2 General Hospital device with product code KKX cleared through the Abbreviated 510(k) pathway after a 242-day FDA review.

K080796 · Sri/Surgical Express · General Hospital
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Nov 2008
Decision
242d
Days
Class 2
Risk

K080796 is an FDA 510(k) clearance for the SRI LP DRAPE. Classified as Drape, Surgical (product code KKX), Class II - Special Controls.

Submitted by Sri/Surgical Express (Austin, US). The FDA issued a Cleared decision on November 17, 2008 after a review of 242 days - an extended review cycle.

This device falls under the General Hospital FDA review panel, regulated under 21 CFR 878.4370 - the FDA general hospital device framework. The Abbreviated 510(k) pathway was used, relying on FDA-recognized standards to demonstrate substantial equivalence.

Device pattern: Standards-based predicate clearance. Standards-verified equivalence. The Abbreviated pathway signals strong alignment with FDA-recognized performance standards - typically associated with lower review burden and faster clearance cycles.

View all Sri/Surgical Express devices

FDA 510(k) Submission Details - K080796

510(k) Number K080796 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 20, 2008
Decision Date November 17, 2008
Days to Decision 242 days
Submission Type Abbreviated
Review Panel General Hospital (HO)
Summary Statement
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
113d slower than avg
Panel avg: 129d · This submission: 242d
Pathway characteristics
Standards-based clearance path.

KKX Device Classification - Class 2, Special Controls

Product Code KKX Drape, Surgical
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 878.4370
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.

Regulatory Peers - KKX Drape, Surgical

All 230
Devices cleared under the same product code (KKX) and FDA review panel - the closest regulatory comparables to K080796.
BUSSE SURGICAL DRAPES III
K092212 · Busse Hospital Disposables, Inc. · Oct 2009
KIMBERLY-CLARK KC100 SURGICAL DRAPES, MODEL KC 100, KIMBERLY-CLARK KC100 SURGICAL EQUIPMENT COVERS, MODEL KC 100
K083234 · Kimberly-Clark Corp. · Mar 2009
BUSSE SURGICAL DRAPE
K082297 · Busse Hospital Disposables, Inc. · Dec 2008
ARROW INTERNATIONAL, INC., SURGICAL DRAPES
K071491 · Arrow Intl., Inc. · Oct 2007
TIBURON DRAPE, MODEL 9349N/ OPTIMA DRAPE, MODEL 9446N
K061762 · Cardinal Health, Inc. · Aug 2006
MICROTEK MEDICAL WARMING DRAPE
K060200 · Microtek Medical, Inc. · May 2006