The following data is part of a premarket notification filed by Toshiba America Medical Systems, Inc. with the FDA for Automatic Image Registration Software, Model Nsfu-050a.
Device ID | K992992 |
510k Number | K992992 |
Device Name: | AUTOMATIC IMAGE REGISTRATION SOFTWARE, MODEL NSFU-050A |
Classification | System, Tomography, Computed, Emission |
Applicant | TOSHIBA AMERICA MEDICAL SYSTEMS, INC. 2441 MICHELLE DR. P.O. BOX 2068 Tustin, CA 92781 -2068 |
Contact | Diana Thorson |
Correspondent | Diana Thorson 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 | 1999-09-07 |
Decision Date | 1999-12-03 |
Summary: | summary |