LUXTEC VIDEOLUX 20/20 CAMERA HEADLIGHT SYSTEM— 510(k) K864381

Name: FDA 510(k) clearance K864381
Creator: U.S. Food and Drug Administration
Published: 1986-12-09

Substantially Equivalent

Luxtec Corp.

FDA 510(k) clearance K864381 for LUXTEC VIDEOLUX 20/20 CAMERA HEADLIGHT SYSTEM, Substantially Equivalent on 1986-12-09. Applicant: Luxtec Corp.. Device class: 1.

Clearance details

Applicant: Luxtec Corp.
Product code: Code FWC
Device class: Class 1
Regulation: 21 CFR 878.4160
Advisory panel: General, Plastic Surgery
Date received: 1986-11-05
Decision date: 1986-12-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Sturbridge, MA, 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.