The following data is part of a premarket notification filed by Fujifilm Medical System U.s.a., Inc. with the FDA for Fuji Medical Laser Imager Mf Print Server Mf-ps667.
Device ID | K970349 |
510k Number | K970349 |
Device Name: | FUJI MEDICAL LASER IMAGER MF PRINT SERVER MF-PS667 |
Classification | System, Image Processing, Radiological |
Applicant | FUJIFILM MEDICAL SYSTEM U.S.A., INC. 333 LUDLOW ST. P.O. BOX 120035 Stamford, CT 06912 -0035 |
Contact | Robert A Uzenoff |
Correspondent | Robert A Uzenoff FUJIFILM MEDICAL SYSTEM U.S.A., INC. 333 LUDLOW ST. P.O. BOX 120035 Stamford, CT 06912 -0035 |
Product Code | LLZ |
CFR Regulation Number | 892.2050 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1997-01-30 |
Decision Date | 1997-03-31 |
Summary: | summary |