KODAK EKTASCAN NETWORK INTERFACE/FOR OTHER MANUFACTURERS— 510(k) K936116

Name: FDA 510(k) clearance K936116
Creator: U.S. Food and Drug Administration
Published: 1994-04-29

Substantially Equivalent

Eastman Kodak Company

FDA 510(k) clearance K936116 for KODAK EKTASCAN NETWORK INTERFACE/FOR OTHER MANUFACTURERS, Substantially Equivalent on 1994-04-29. Applicant: Eastman Kodak Company. Device class: 1.

Clearance details

Applicant: Eastman Kodak Company
Product code: Code LMD
Device class: Class 1
Regulation: 21 CFR 892.2020
Advisory panel: Radiology
Date received: 1993-12-23
Decision date: 1994-04-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Rochester, NY, 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 Eastman Kodak Company

view all

K060550 — KODAK DIRECTVIEW DR 3000 SYSTEM 64KW/80KW GENERATORS, MODELS 6551345, 65513862006-03-31
K060137 — KODAK ECLIPSE IMAGE PROCESSING SOFTWARE2006-03-16
K060079 — KODAK MODEL CR-7400 DIGITAL RADIOGRAPHY SYSTEM2006-02-08
K060055 — KODAK PACS2006-02-07
K053347 — KODAK CARESTREAM PACS2006-01-04

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