Cleared Traditional

K060153 - ACUMED LASER, MODEL 1000

K060153 is an FDA 510(k) clearance for ACUMED LASER, manufactured by Laser Thera, LLC. The device is a Class 2 Physical Medicine device with product code ILY cleared through the Traditional 510(k) pathway after a 252-day FDA review.

K060153 · Laser Thera, LLC · Physical Medicine device
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Sep 2006
Decision
252d
Days
Class 2
Risk

K060153 is an FDA 510(k) clearance for the ACUMED LASER, MODEL 1000. Classified as Lamp, Infrared, Therapeutic Heating (product code ILY), Class II - Special Controls.

Submitted by Laser Thera, LLC (Yukon, US). The FDA issued a Cleared decision on September 29, 2006 after a review of 252 days - an extended review 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: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Physical Medicine review framework, consistent with the majority of Class II 510(k) submissions.

View all Laser Thera, LLC devices

FDA 510(k) Submission Details - K060153

510(k) Number K060153 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 20, 2006
Decision Date September 29, 2006
Days to Decision 252 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
137d slower than avg
Panel avg: 115d · This submission: 252d
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 45
Devices cleared under the same product code (ILY) and FDA review panel - the closest regulatory comparables to K060153.
THERMAPULSE
K092222 · Palomar Medical Products, Inc. · Aug 2009
AKLARUS PHOTOTHERAPY SYSTEM
K083183 · Hill Laboratories Co. · Jul 2009
EZLASE
K083595 · Biolase Technology, Inc. · Apr 2009
DYNATRON DX2 TRACTION UNIT
K051680 · Dynatronics Corp. · Oct 2005
HILT FAMILY LASER: HILT I, HILT II, HILT III
K051537 · Cynosure, Inc. · Sep 2005
ASA 'M FAMILY' DIODE LASER, MODEL MI, MIX5, M6
K051922 · Cynosure, Inc. · Sep 2005