PERIKON PCL 90— 510(k) K922294

Substantially Equivalent

Optikon Oftalmologia Spa

FDA 510(k) clearance K922294 for PERIKON PCL 90, Substantially Equivalent on 1993-01-28. Applicant: Optikon Oftalmologia Spa. Device class: 1.

Clearance details

Applicant: Optikon Oftalmologia Spa
Product code: Code HPT
Device class: Class 1
Regulation: 21 CFR 886.1605
Advisory panel: Ophthalmic
Date received: 1992-05-15
Decision date: 1993-01-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Sandy, UT, 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.