KODAK EKTASCAN VIDEO CAMERA & COMPACT VIDEO CAMERA— 510(k) K860691

Name: FDA 510(k) clearance K860691
Creator: U.S. Food and Drug Administration
Published: 1986-03-13

Substantially Equivalent

Eastman Kodak Company

FDA 510(k) clearance K860691 for KODAK EKTASCAN VIDEO CAMERA & COMPACT VIDEO CAMERA, Substantially Equivalent on 1986-03-13. Applicant: Eastman Kodak Company. Device class: 2.

Clearance details

Applicant: Eastman Kodak Company
Product code: Code LMC
Device class: Class 2
Regulation: 21 CFR 892.2040
Advisory panel: Radiology
Date received: 1986-02-25
Decision date: 1986-03-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Rochester, NY, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code LMC

view all

K141346 — SONY HYBIRD GRAPHIC UP-971AD, SONY HYBIRD GRAPHIC PRINTER UP-991AD2014-06-26
K141454 — SONY DIGITAL PRINTER UP-D898MD/SONY HYBRID PRINTER UP-X898MD2014-06-26
K111566 — DRYVIEW CHROMA IMAGING SYSTEM2011-10-06
K092280 — CYPHER DICOM PRINT SOLUTION2009-10-16
K090469 — CARESTREAM DRYVIEW 5850 LASER IMAGER2009-05-22

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.