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..

Clearance details

Applicant: Verg, Inc.
Product code: Code FXN
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 ↗

Recent devices under product code FXN

K131596 — WOUND MEASURING & MONITORING DEVICE2013-12-11
K130165 — PICTZAR DIGITAL PLANIMETRY SOFTWARE APPLICATION 7.02013-08-30
K070426 — SILHOUETTE, MODEL 1000.012007-06-29

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