The following data is part of a premarket notification filed by Fujifilm Medical System U.s.a., Inc. with the FDA for Fuji Fcr Image Processing Unit Ip-u515.
Device ID | K942561 |
510k Number | K942561 |
Device Name: | FUJI FCR IMAGE PROCESSING UNIT IP-U515 |
Classification | System, Imaging, X-ray, Electrostatic |
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 | IXK |
CFR Regulation Number | 892.1630 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1994-05-31 |
Decision Date | 1994-12-23 |