NIDEK AR-1200— 510(k) K890559

Substantially Equivalent

Nidek, Inc.

FDA 510(k) clearance K890559 for NIDEK AR-1200, Substantially Equivalent on 1989-02-27. Applicant: Nidek, Inc..

Clearance details

Applicant: Nidek, Inc.
Product code: Code HKO
Advisory panel: Ophthalmic
Date received: 1989-02-06
Decision date: 1989-02-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Palo Alto, CA, US

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