The following data is part of a premarket notification filed by Siemens Medical Solutions Usa, Inc. with the FDA for Biograph Mct Family Of Pet/ct Systems.
Device ID | K173578 |
510k Number | K173578 |
Device Name: | Biograph MCT Family Of PET/CT Systems |
Classification | System, Tomography, Computed, Emission |
Applicant | Siemens Medical Solutions USA, Inc. 810 Innovation Drive Knoxville, TN 37932 |
Contact | Tabitha Estes |
Correspondent | Tabitha Estes Siemens Medical Solutions USA, Inc. 810 Innovation Drive Knoxville, TN 37932 |
Product Code | KPS |
CFR Regulation Number | 892.1200 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2017-11-20 |
Decision Date | 2017-12-20 |
Summary: | summary |