VIDEO VISION ANALYZER (VIVA), VRB 100— 510(k) K945959

Name: FDA 510(k) clearance K945959
Creator: U.S. Food and Drug Administration
Published: 1995-03-01

Substantially Equivalent

Tomey Corporation USA

FDA 510(k) clearance K945959 for VIDEO VISION ANALYZER (VIVA), VRB 100, Substantially Equivalent on 1995-03-01. Applicant: Tomey Corporation USA. Device class: 1.

Clearance details

Applicant: Tomey Corporation USA
Product code: Code HKO
Device class: Class 1
Regulation: 21 CFR 886.1760
Advisory panel: Ophthalmic
Date received: 1994-12-07
Decision date: 1995-03-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Cambridge, MA, 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.