The following data is part of a premarket notification filed by Shimadzu Medical Systems with the FDA for Shimadzu Whole Body X-ray Ct Scanner Sct-3000te.
Device ID | K894888 |
510k Number | K894888 |
Device Name: | SHIMADZU WHOLE BODY X-RAY CT SCANNER SCT-3000TE |
Classification | System, X-ray, Tomography, Computed |
Applicant | SHIMADZU MEDICAL SYSTEMS 101 WEST WALNUT ST. Gardenia, CA 90248 |
Contact | De Mint |
Correspondent | De Mint SHIMADZU MEDICAL SYSTEMS 101 WEST WALNUT ST. Gardenia, CA 90248 |
Product Code | JAK |
CFR Regulation Number | 892.1750 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1989-08-01 |
Decision Date | 1990-01-23 |