VARICOSCREEN(TM)— 510(k) K900404

Substantially Equivalent

Promedex, Inc.

FDA 510(k) clearance K900404 for VARICOSCREEN(TM), Substantially Equivalent on 1990-12-07. Applicant: Promedex, Inc..

Clearance details

Applicant: Promedex, Inc.
Product code: Code KYA
Advisory panel: Obstetrics/Gynecology
Date received: 1990-01-29
Decision date: 1990-12-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Fort Woth, TX, US

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