DURETTE OCULAR IMPLANT— 510(k) K123764

Substantially Equivalent

Oculo-Plastik, Inc.

FDA 510(k) clearance K123764 for DURETTE OCULAR IMPLANT, Substantially Equivalent on 2013-01-31. Applicant: Oculo-Plastik, Inc..

Clearance details

Applicant: Oculo-Plastik, Inc.
Product code: Code HPZ
Advisory panel: Ophthalmic
Date received: 2012-12-07
Decision date: 2013-01-31
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Montreal, Qc, CA

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