COMPASS— 510(k) K150320

Substantially Equivalent

Centervue S.P.A.

FDA 510(k) clearance K150320 for COMPASS, Substantially Equivalent on 2015-06-30. Applicant: Centervue S.P.A..

Clearance details

Applicant: Centervue S.P.A.
Product code: Code MYC
Advisory panel: Ophthalmic
Date received: 2015-02-09
Decision date: 2015-06-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Padova, IT

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