The following data is part of a premarket notification filed by Kodak Health Imaging Systems, Inc. with the FDA for Kodak Ektascan Triad Laser Printer System, Photon Laser Printer.
Device ID | K951807 |
510k Number | K951807 |
Device Name: | KODAK EKTASCAN TRIAD LASER PRINTER SYSTEM, PHOTON LASER PRINTER |
Classification | Camera, Multi Format, Radiological |
Applicant | KODAK HEALTH IMAGING SYSTEMS, INC. 18325 WATERVIEW PKWY. Dallas, TX 75252 |
Contact | Carl Alletto |
Correspondent | Carl Alletto KODAK HEALTH IMAGING SYSTEMS, INC. 18325 WATERVIEW PKWY. Dallas, TX 75252 |
Product Code | LMC |
CFR Regulation Number | 892.2040 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1995-04-19 |
Decision Date | 1995-09-13 |