The following data is part of a premarket notification filed by Toshiba America Medical Systems, Inc. with the FDA for Tsx-101a/a And Tsx-101a/c Aquilion Multislice Ct Scanners.
| Device ID | K033418 |
| 510k Number | K033418 |
| Device Name: | TSX-101A/A AND TSX-101A/C AQUILION MULTISLICE CT SCANNERS |
| Classification | System, X-ray, Tomography, Computed |
| Applicant | TOSHIBA AMERICA MEDICAL SYSTEMS, INC. 2441 MICHELLE DR. P.O. BOX 2068 Tustin, CA 92781 -2068 |
| Contact | Paul Biggins |
| Product Code | JAK |
| CFR Regulation Number | 892.1750 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | Yes |
| Combination Product | No |
| Date Received | 2003-10-27 |
| Decision Date | 2003-11-10 |
| Summary: | summary |