HA ORBITAL IMPLANT— 510(k) K021643

Substantially Equivalent

Laboratoire Villanova

FDA 510(k) clearance K021643 for HA ORBITAL IMPLANT, Substantially Equivalent on 2002-12-13. Applicant: Laboratoire Villanova. Device class: 2.

Clearance details

Applicant: Laboratoire Villanova
Product code: Code HPZ
Device class: Class 2
Regulation: 21 CFR 886.3320
Advisory panel: Ophthalmic
Date received: 2002-05-20
Decision date: 2002-12-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Le Touquet, FR

Download summary PDF View on FDA.gov ↗

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