NEW IOWA MOTILITY IMPLANT— 510(k) K900080

Substantially Equivalent

Oculo Plastik, Inc.

FDA 510(k) clearance K900080 for NEW IOWA MOTILITY IMPLANT, Substantially Equivalent on 1990-03-23. Applicant: Oculo Plastik, Inc..

Clearance details

Applicant: Oculo Plastik, Inc.
Product code: Code HPZ
Advisory panel: Ophthalmic
Date received: 1990-01-04
Decision date: 1990-03-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Montreal, Quebec Canada, CA

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