VIVASCOPE SYSTEM, MODEL 1500, 3000— 510(k) K080788

Substantially Equivalent

Lucid, Inc.

FDA 510(k) clearance K080788 for VIVASCOPE SYSTEM, MODEL 1500, 3000, Substantially Equivalent on 2008-09-17. Applicant: Lucid, Inc.. Device class: 2.

Clearance details

Applicant: Lucid, Inc.
Product code: Code PSN
Device class: Class 2
Regulation: 21 CFR 878.4580
Advisory panel: General, Plastic Surgery
Date received: 2008-03-20
Decision date: 2008-09-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Rochester, NY, 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.