Cleared Traditional

K112811 - SANICLAVE 200

K112811 is an FDA 510(k) clearance for SANICLAVE 200, manufactured by Alternative Pioneering Research and Development. The device is a Class 2 General Hospital device with product code FLE cleared through the Traditional 510(k) pathway after a 106-day FDA review.

K112811 · Alternative Pioneering Research and Development · General Hospital
Download Printable Device Report (PDF)
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Jan 2012
Decision
106d
Days
Class 2
Risk

K112811 is an FDA 510(k) clearance for the SANICLAVE 200. Classified as Sterilizer, Steam (product code FLE), Class II - Special Controls.

Submitted by Alternative Pioneering Research and Development (Shafer, US). The FDA issued a Cleared decision on January 11, 2012 after a review of 106 days - within the typical 510(k) review window.

This device falls under the General Hospital FDA review panel, regulated under 21 CFR 880.6880 - 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 Alternative Pioneering Research and Development devices

FDA 510(k) Submission Details - K112811

510(k) Number K112811 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 27, 2011
Decision Date January 11, 2012
Days to Decision 106 days
Submission Type Traditional
Review Panel General Hospital (HO)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
23d faster than avg
Panel avg: 129d · This submission: 106d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

FLE Device Classification - Class 2, Special Controls

Product Code FLE Sterilizer, Steam
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 880.6880
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 - FLE Sterilizer, Steam

All 87
Devices cleared under the same product code (FLE) and FDA review panel - the closest regulatory comparables to K112811.
Family of Steam sterilizers B17 B22 Series
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K112403 · STERIS Corporation · May 2012
AMSCO CHIMERON MEDIUM STEAM STERILIZER
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AMSCO CHIMERON SMALL STEAM STERILIZER
K111223 · STERIS Corporation · Sep 2011
AMSCO EVOLUTION SERIES STEAM STERILIZER, MODEL: HC-2000 AND HC-3000
K092490 · STERIS Corporation · Nov 2009