STREAK RETINOSCOPE RX-RP— 510(k) K950795

Substantially Equivalent

Neitz Instruments Company, Ltd.

FDA 510(k) clearance K950795 for STREAK RETINOSCOPE RX-RP, Substantially Equivalent on 1995-03-28. Applicant: Neitz Instruments Company, Ltd..

Clearance details

Applicant: Neitz Instruments Company, Ltd.
Product code: Code HKM
Advisory panel: Ophthalmic
Date received: 1995-02-21
Decision date: 1995-03-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Tokyo, JP

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