MP-1 MICRO PERIMETER— 510(k) K023719

Substantially Equivalent

Nidek Technologies Srl

FDA 510(k) clearance K023719 for MP-1 MICRO PERIMETER, Substantially Equivalent on 2002-12-23. Applicant: Nidek Technologies Srl. Device class: 2.

Clearance details

Applicant: Nidek Technologies Srl
Product code: Code HKI
Device class: Class 2
Regulation: 21 CFR 886.1120
Advisory panel: Ophthalmic
Date received: 2002-11-05
Decision date: 2002-12-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Vigonza (Padova), IT

Download summary PDF View on FDA.gov ↗

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