Cleared Traditional

K113131 - LIASYS 450

K113131 is an FDA 510(k) clearance for LIASYS 450, manufactured by Ams. The device is a Class 2 Chemistry device with product code CFR cleared through the Traditional 510(k) pathway after a 136-day FDA review.

K113131 · Ams · Chemistry device
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Mar 2012
Decision
136d
Days
Class 2
Risk

K113131 is an FDA 510(k) clearance for the LIASYS 450. Classified as Hexokinase, Glucose (product code CFR), Class II - Special Controls.

Submitted by Ams (Guidonia, Rome, IT). The FDA issued a Cleared decision on March 8, 2012 after a review of 136 days - within the typical 510(k) review window.

This device falls under the Chemistry FDA review panel, regulated under 21 CFR 862.1345 - the FDA in vitro diagnostics and chemistry 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 Chemistry review framework, consistent with the majority of Class II 510(k) submissions.

FDA 510(k) Submission Details - K113131

510(k) Number K113131 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received October 24, 2011
Decision Date March 08, 2012
Days to Decision 136 days
Submission Type Traditional
Review Panel Chemistry (CH)
Summary Statement
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
48d slower than avg
Panel avg: 88d · This submission: 136d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

CFR Device Classification - Class 2, Special Controls

Product Code CFR Hexokinase, Glucose
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 862.1345
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 Chemistry devices follow this clearance model.

Regulatory Peers - CFR Hexokinase, Glucose

All 139
Devices cleared under the same product code (CFR) and FDA review panel - the closest regulatory comparables to K113131.
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