KODAK EKTACHEM CLINICAL CHEMISTRY SLIDES— 510(k) K912217

Name: FDA 510(k) clearance K912217
Creator: U.S. Food and Drug Administration
Published: 1991-07-01

Substantially Equivalent

Eastman Kodak Company

FDA 510(k) clearance K912217 for KODAK EKTACHEM CLINICAL CHEMISTRY SLIDES, Substantially Equivalent on 1991-07-01. Applicant: Eastman Kodak Company. Device class: 1.

Clearance details

Applicant: Eastman Kodak Company
Product code: Code DIH
Device class: Class 1
Regulation: 21 CFR 862.3240
Advisory panel: Clinical Toxicology
Date received: 1991-05-20
Decision date: 1991-07-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Rochester, NY, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code DIH

view all

K103373 — SYNCHRON SYSTEMS CHOLINESTERASE (CHEX) MODEL A537222011-02-07
K061093 — CHOLINESTERASE GEN.2 TEST SYSTEM2006-07-03
K051444 — SENTINEL CHOLINESTERASE LIQUID2005-06-20
K030045 — OLYMPUS CHOLINESTERASE REAGENT (CATALOG NUMBER OSR6114)2003-02-21
K023992 — WIENER LAB COLINESTERASA AA2003-02-12

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.