The following data is part of a premarket notification filed by Shimadzu Corp. with the FDA for Shimadzu Whole Body X-ray Ct Scanner Sct-4800tf.
Device ID | K935487 |
510k Number | K935487 |
Device Name: | SHIMADZU WHOLE BODY X-RAY CT SCANNER SCT-4800TF |
Classification | System, X-ray, Tomography, Computed |
Applicant | SHIMADZU CORP. 20101 SOUTH VERMONT AVE. Torrance, CA 90502 -1328 |
Contact | Michael Fishback |
Correspondent | Michael Fishback SHIMADZU CORP. 20101 SOUTH VERMONT AVE. Torrance, CA 90502 -1328 |
Product Code | JAK |
CFR Regulation Number | 892.1750 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1993-11-15 |
Decision Date | 1994-07-05 |