VISTA ILLUMINATION SYSTEM— 510(k) K970217

Name: FDA 510(k) clearance K970217
Creator: U.S. Food and Drug Administration
Published: 1997-04-02

Substantially Equivalent

Vista Medical Technologies, Inc.

FDA 510(k) clearance K970217 for VISTA ILLUMINATION SYSTEM, Substantially Equivalent on 1997-04-02. Applicant: Vista Medical Technologies, Inc.. Device class: 2.

Clearance details

Applicant: Vista Medical Technologies, Inc.
Product code: Code FFS
Device class: Class 2
Regulation: 21 CFR 876.1500
Advisory panel: Gastroenterology, Urology
Date received: 1997-01-21
Decision date: 1997-04-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Westborough, 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.