TRILUMINA THERAPEUTIC LASER SYSTEM— 510(k) K023935

Name: FDA 510(k) clearance K023935
Creator: U.S. Food and Drug Administration
Published: 2003-01-28

Substantially Equivalent

Texas Applied Biomedical Services

FDA 510(k) clearance K023935 for TRILUMINA THERAPEUTIC LASER SYSTEM, Substantially Equivalent on 2003-01-28. Applicant: Texas Applied Biomedical Services. Device class: 2.

Clearance details

Applicant: Texas Applied Biomedical Services
Product code: Code NHN
Device class: Class 2
Regulation: 21 CFR 890.5500
Advisory panel: Physical Medicine
Date received: 2002-11-26
Decision date: 2003-01-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Houston, TX, US

Download summary PDF View on FDA.gov ↗

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