Cleared Traditional

K091285 - AL T LASER, MODEL AVI HPLL-12

K091285 is an FDA 510(k) clearance for AL T LASER, manufactured by Avicenna Laser Technology, Inc.. The device is a Class 2 Physical Medicine device with product code ILY cleared through the Traditional 510(k) pathway after a 88-day FDA review.

K091285 · Avicenna Laser Technology, Inc. · Physical Medicine device
Download Printable Device Report (PDF)
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Jul 2009
Decision
88d
Days
Class 2
Risk

K091285 is an FDA 510(k) clearance for the AL T LASER, MODEL AVI HPLL-12. Classified as Lamp, Infrared, Therapeutic Heating (product code ILY), Class II - Special Controls.

Submitted by Avicenna Laser Technology, Inc. (Chagrin Falls, US). The FDA issued a Cleared decision on July 28, 2009 after a review of 88 days - a notably fast clearance cycle.

This device falls under the Physical Medicine FDA review panel, regulated under 21 CFR 890.5500 - the FDA physical medicine 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: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

View all Avicenna Laser Technology, Inc. devices

FDA 510(k) Submission Details - K091285

510(k) Number K091285 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 01, 2009
Decision Date July 28, 2009
Days to Decision 88 days
Submission Type Traditional
Review Panel Physical Medicine (PM)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
27d faster than avg
Panel avg: 115d · This submission: 88d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

ILY Device Classification - Class 2, Special Controls

Product Code ILY Lamp, Infrared, Therapeutic Heating
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 890.5500
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 Physical Medicine devices follow this clearance model.

Regulatory Peers - ILY Lamp, Infrared, Therapeutic Heating

All 38
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