FIBERLUME— 510(k) K901108

Substantially Equivalent

Burton

FDA 510(k) clearance K901108 for FIBERLUME, Substantially Equivalent on 1990-03-28. Applicant: Burton. Device class: 2.

Clearance details

Applicant: Burton
Product code: Code HBI
Device class: Class 2
Regulation: 21 CFR 878.4580
Advisory panel: General, Plastic Surgery
Date received: 1990-03-09
Decision date: 1990-03-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Van Nuys, CA, 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.