The following data is part of a premarket notification filed by Siemens Medical Solutions Usa, Inc. with the FDA for Quiet/silent Scanning Suite.
Device ID | K132831 |
510k Number | K132831 |
Device Name: | QUIET/SILENT SCANNING SUITE |
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 | No |
Date Received | 2013-09-10 |
Decision Date | 2013-11-01 |
Summary: | summary |