LTU-904 PORTABLE LASER THERAPY UNIT— 510(k) K030295

Name: FDA 510(k) clearance K030295
Creator: U.S. Food and Drug Administration
Published: 2004-12-23

Substantially Equivalent

Riancorp Pty, Ltd.

FDA 510(k) clearance K030295 for LTU-904 PORTABLE LASER THERAPY UNIT, Substantially Equivalent on 2004-12-23. Applicant: Riancorp Pty, Ltd.. Device class: 2.

Clearance details

Applicant: Riancorp Pty, Ltd.
Product code: Code NZY
Device class: Class 2
Regulation: 21 CFR 890.5500
Advisory panel: Physical Medicine
Date received: 2003-01-28
Decision date: 2004-12-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Leesburg, FL, US

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