Cleared Traditional

K060134 - APOLLO IR HEAT LAMP SYSTEM

K060134 is an FDA 510(k) clearance for APOLLO IR HEAT LAMP SYSTEM, manufactured by Apollo Physical Therapy Products International. The device is a Class 2 Physical Medicine device with product code ILY cleared through the Traditional 510(k) pathway after a 62-day FDA review.

K060134 · Apollo Physical Therapy Products International · Physical Medicine device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Mar 2006
Decision
62d
Days
Class 2
Risk

K060134 is an FDA 510(k) clearance for the APOLLO IR HEAT LAMP SYSTEM. Classified as Lamp, Infrared, Therapeutic Heating (product code ILY), Class II - Special Controls.

Submitted by Apollo Physical Therapy Products International (Houston, US). The FDA issued a Cleared decision on March 21, 2006 after a review of 62 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 Apollo Physical Therapy Products International devices

FDA 510(k) Submission Details - K060134

510(k) Number K060134 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 18, 2006
Decision Date March 21, 2006
Days to Decision 62 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
53d faster than avg
Panel avg: 115d · This submission: 62d
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 53
Devices cleared under the same product code (ILY) and FDA review panel - the closest regulatory comparables to K060134.
THERMAPULSE
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K051922 · Cynosure, Inc. · Sep 2005