VERGE VIDEOMETER— 510(k) K962148

Substantially Equivalent

Verg, Inc.

FDA 510(k) clearance K962148 for VERGE VIDEOMETER, Substantially Equivalent on 1996-12-20. Applicant: Verg, Inc.. Device class: 1.

Clearance details

Applicant: Verg, Inc.
Product code: Code FXN
Device class: Class 1
Regulation: 21 CFR 878.4160
Advisory panel: General, Plastic Surgery
Date received: 1996-06-03
Decision date: 1996-12-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Winnipeg, Manitoba, CA

Download summary PDF View on FDA.gov ↗

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