KODAK X-OMATIC IDENTIFICATION CAMERA DIGITAL— 510(k) K870701

Name: FDA 510(k) clearance K870701
Creator: U.S. Food and Drug Administration
Published: 1987-02-26

Substantially Equivalent

Eastman Kodak Company

FDA 510(k) clearance K870701 for KODAK X-OMATIC IDENTIFICATION CAMERA DIGITAL, Substantially Equivalent on 1987-02-26. Applicant: Eastman Kodak Company. Device class: 1.

Clearance details

Applicant: Eastman Kodak Company
Product code: Code JAC
Device class: Class 1
Regulation: 21 CFR 892.1640
Advisory panel: Radiology
Date received: 1987-02-20
Decision date: 1987-02-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Rochester, NY, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code JAC

view all

K942883 — DIGITAL I.D. CAMERA1994-09-30
K930752 — CT/MRI TOPOGRAPHIC MARKER1993-11-19
K932357 — FUJI EC ID CAMERA1993-07-26
K925892 — SOLSTICE XRAY RING MARKER PAD1993-05-18
K923533 — ADMARK1993-03-04

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.