OPTIFIELD I AND II AUTOMATED PERIMETERS— 510(k) K884867

Name: FDA 510(k) clearance K884867
Creator: U.S. Food and Drug Administration
Published: 1989-03-09

Substantially Equivalent

Optimed, Inc.

FDA 510(k) clearance K884867 for OPTIFIELD I AND II AUTOMATED PERIMETERS, Substantially Equivalent on 1989-03-09. Applicant: Optimed, Inc.. Device class: 1.

Clearance details

Applicant: Optimed, Inc.
Product code: Code HPT
Device class: Class 1
Regulation: 21 CFR 886.1605
Advisory panel: Ophthalmic
Date received: 1988-11-21
Decision date: 1989-03-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Oakland, CA, 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.