The following data is part of a premarket notification filed by Siemens Medical Solutions Usa Inc. with the FDA for Magnetom Spectra.
Device ID | K121160 |
510k Number | K121160 |
Device Name: | MAGNETOM SPECTRA |
Classification | System, Nuclear Magnetic Resonance Imaging |
Applicant | SIEMENS MEDICAL SOLUTIONS USA INC. 51 VALLEY STREAM PARKWAY Malvern, PA 19355 |
Contact | Nadia Sookdeo |
Correspondent | Nadia Sookdeo SIEMENS MEDICAL SOLUTIONS USA INC. 51 VALLEY STREAM PARKWAY Malvern, PA 19355 |
Product Code | LNH |
CFR Regulation Number | 892.1000 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | Yes |
Date Received | 2012-04-16 |
Decision Date | 2012-07-16 |
Summary: | summary |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() MAGNETOM SPECTRA 79106773 4181473 Live/Registered |
Siemens Healthcare GmbH 2011-10-20 |