CENTERVUE DIGITAL RETINOGRAPHY SYSTEM— 510(k) K101935

Substantially Equivalent

Centervue S.P.A.

FDA 510(k) clearance K101935 for CENTERVUE DIGITAL RETINOGRAPHY SYSTEM, Substantially Equivalent on 2010-10-27. Applicant: Centervue S.P.A..

Clearance details

Applicant: Centervue S.P.A.
Product code: Code HKI
Advisory panel: Ophthalmic
Date received: 2010-07-12
Decision date: 2010-10-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Rome, IT

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