KODAK AUTOMIXER II PLUS

Processor, Radiographic-film, Automatic

EASTMAN KODAK COMPANY

The following data is part of a premarket notification filed by Eastman Kodak Company with the FDA for Kodak Automixer Ii Plus.

Pre-market Notification Details

Device IDK954484
510k NumberK954484
Device Name:KODAK AUTOMIXER II PLUS
ClassificationProcessor, Radiographic-film, Automatic
Applicant EASTMAN KODAK COMPANY 901 ELMGROVE RD. Rochester,  NY  14653 -0002
ContactDennis E Sneddon
CorrespondentDennis E Sneddon
EASTMAN KODAK COMPANY 901 ELMGROVE RD. Rochester,  NY  14653 -0002
Product CodeIXW  
CFR Regulation Number892.1900 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1995-09-27
Decision Date1995-10-18

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.