Cleared Traditional

K032787 - NEUROLASE, MODELS 150V, 150C, 1064

K032787 is an FDA 510(k) clearance for NEUROLASE, manufactured by Spectrum Laser & Technologies. The device is a Class 2 Physical Medicine device with product code ILY cleared through the Traditional 510(k) pathway after a 73-day FDA review.

K032787 · Spectrum Laser & Technologies · Physical Medicine device
Download Printable Device Report (PDF) Official FDA 510(k) Summary (PDF)
Optimized for regulatory review, auditing and printing
Nov 2003
Decision
73d
Days
Class 2
Risk

K032787 is an FDA 510(k) clearance for the NEUROLASE, MODELS 150V, 150C, 1064. Classified as Lamp, Infrared, Therapeutic Heating (product code ILY), Class II - Special Controls.

Submitted by Spectrum Laser & Technologies (Colorado Springs, US). The FDA issued a Cleared decision on November 20, 2003 after a review of 73 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.

FDA 510(k) Submission Details - K032787

510(k) Number K032787 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 08, 2003
Decision Date November 20, 2003
Days to Decision 73 days
Submission Type Traditional
Review Panel Physical Medicine (PM)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
43d faster than avg
Panel avg: 116d · This submission: 73d
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 228
Devices cleared under the same product code (ILY) and FDA review panel - the closest regulatory comparables to K032787.
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K032787 · NEUROLASE, MODELS 150V, 150C, 1064
Download PDF FDA Summary Spectrum Laser & Tech…