ACULUX, MODEL AX3001, AX3002— 510(k) K001223

Substantially Equivalent

Aculux

FDA 510(k) clearance K001223 for ACULUX, MODEL AX3001, AX3002, Substantially Equivalent on 2000-06-23. Applicant: Aculux. Device class: 2.

Clearance details

Applicant: Aculux
Product code: Code FQP
Device class: Class 2
Regulation: 21 CFR 878.4580
Advisory panel: General, Plastic Surgery
Date received: 2000-04-17
Decision date: 2000-06-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Naples, FL, 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.