POWER LASER 90— 510(k) K030692

Substantially Equivalent

Andi Electromedical Aps

FDA 510(k) clearance K030692 for POWER LASER 90, Substantially Equivalent on 2003-07-17. Applicant: Andi Electromedical Aps. Device class: 2.

Clearance details

Applicant: Andi Electromedical Aps
Product code: Code NHN
Device class: Class 2
Regulation: 21 CFR 890.5500
Advisory panel: Physical Medicine
Date received: 2003-03-05
Decision date: 2003-07-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Carmel, IN, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.