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.. Device class: 1.

Clearance details

Applicant: Promedex, Inc.
Product code: Code KYA
Device class: Class 1
Regulation: 21 CFR 884.2982
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

Download summary PDF View on FDA.gov ↗

Recent devices under product code KYA

K832989 — BREAST THERMAL ACTIVITY INDICATOR1984-01-17
K823245 — THERMAX; THERMAX SYSTEM1982-11-16
K821524 — CHIROPRATIC INFRA-RED CRYSTAL PAK1982-09-08
K821049 — PARATHERM1982-04-29

More clearances from Promedex, Inc.

K914407 — PROMOGLASS(TM) SUNGLASSES (NON-PRESCRIPTION)1991-12-31
K905764 — SEMINOR1991-03-12

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