VORTECH'S AUTOROUTER (AUTOMATIC IMAGE ROUTING)— 510(k) K925097

Name: FDA 510(k) clearance K925097
Creator: U.S. Food and Drug Administration
Published: 1993-01-15

Substantially Equivalent

Vortech Data, Inc.

FDA 510(k) clearance K925097 for VORTECH'S AUTOROUTER (AUTOMATIC IMAGE ROUTING), Substantially Equivalent on 1993-01-15. Applicant: Vortech Data, Inc.. Device class: 1.

Clearance details

Applicant: Vortech Data, Inc.
Product code: Code LMD
Device class: Class 1
Regulation: 21 CFR 892.2020
Advisory panel: Radiology
Date received: 1992-10-08
Decision date: 1993-01-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Richardson, TX, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code LMD

view all

K994329 — IIVS INTEGRATED IMAGE VIEWING STATION2000-05-26
K992698 — STENTOR, PAGEVIEW1999-10-25
K992426 — RAYPAX WEB CLINICAL SYSTEM1999-10-13
K992352 — ITR2000: INTERNET TELERADIOLOGY, MODEL RELEASE 1.01999-09-29
K991537 — SAMSUNG RAYPAX SYSTEM1999-07-06

More clearances from Vortech Data, Inc.

view all

K924366 — PERSONAL DISPLAY SYSTEM1993-04-07
K924229 — VG-A MIG1992-11-27
K922310 — VORTECH'S PERSONAL DISPLAY SYSTEM1992-07-30
K915362 — VORTECH'S FILM DIGITIZER, FD-11992-04-06
K914834 — VORTECH 3M NETWORK PRINTING1992-03-06

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