MaxiTears Contacts PF— 510(k) K182984

Substantially Equivalent

Omnivision AG

FDA 510(k) clearance K182984 for MaxiTears Contacts PF, Substantially Equivalent on 2019-07-24. Applicant: Omnivision AG. Device class: 2.

Clearance details

Applicant: Omnivision AG
Product code: Code MRC
Device class: Class 2
Regulation: 21 CFR 886.5918
Advisory panel: Ophthalmic
Date received: 2018-10-29
Decision date: 2019-07-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Neuhausen Am Rheinfall, CH

Download summary PDF View on FDA.gov ↗

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