RICHMOND VISUAL FIELD SCREENER— 510(k) K873912

Name: FDA 510(k) clearance K873912
Creator: U.S. Food and Drug Administration
Published: 1987-11-02

Substantially Equivalent

Richmond Products, Inc.

FDA 510(k) clearance K873912 for RICHMOND VISUAL FIELD SCREENER, Substantially Equivalent on 1987-11-02. Applicant: Richmond Products, Inc.. Device class: 1.

Clearance details

Applicant: Richmond Products, Inc.
Product code: Code HOO
Device class: Class 1
Regulation: 21 CFR 886.1605
Advisory panel: Ophthalmic
Date received: 1987-09-25
Decision date: 1987-11-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Boca Raton, FL, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.