The following data is part of a premarket notification filed by Eastman Kodak Company with the FDA for Kodak Automixer Ii Plus.
Device ID | K954484 |
510k Number | K954484 |
Device Name: | KODAK AUTOMIXER II PLUS |
Classification | Processor, Radiographic-film, Automatic |
Applicant | EASTMAN KODAK COMPANY 901 ELMGROVE RD. Rochester, NY 14653 -0002 |
Contact | Dennis E Sneddon |
Correspondent | Dennis E Sneddon EASTMAN KODAK COMPANY 901 ELMGROVE RD. Rochester, NY 14653 -0002 |
Product Code | IXW |
CFR Regulation Number | 892.1900 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1995-09-27 |
Decision Date | 1995-10-18 |