The following data is part of a premarket notification filed by Toshiba America Medical Systems, Inc. with the FDA for Transview (transmission System),model Ndtr-701a.
| Device ID | K982300 |
| 510k Number | K982300 |
| Device Name: | TRANSVIEW (TRANSMISSION SYSTEM),MODEL NDTR-701A |
| Classification | System, Tomography, Computed, Emission |
| Applicant | TOSHIBA AMERICA MEDICAL SYSTEMS, INC. 2441 MICHELLE DR. P.O. BOX 2068 Tustin, CA 92781 -2068 |
| Contact | Donelle Krajewski |
| Correspondent | Donelle Krajewski TOSHIBA AMERICA MEDICAL SYSTEMS, INC. 2441 MICHELLE DR. P.O. BOX 2068 Tustin, CA 92781 -2068 |
| Product Code | KPS |
| CFR Regulation Number | 892.1200 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1998-07-01 |
| Decision Date | 1998-09-25 |
| Summary: | summary |