The following data is part of a premarket notification filed by Siemens Ag, Medical Solutions with the FDA for Syngo Volume Perfusion-ct Neuro.
Device ID | K073238 |
510k Number | K073238 |
Device Name: | SYNGO VOLUME PERFUSION-CT NEURO |
Classification | System, X-ray, Tomography, Computed |
Applicant | SIEMENS AG, MEDICAL SOLUTIONS HENKESTRASSE 127 Erlangen, DE 91052 |
Contact | Ralf Hofmann |
Correspondent | Stefan Preiss TUV SUD AMERICA INC. 1775 OLD HIGHWAY 8 NW New Brighton, MN 55112 -1891 |
Product Code | JAK |
CFR Regulation Number | 892.1750 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | Yes |
Combination Product | No |
Date Received | 2007-11-16 |
Decision Date | 2008-01-03 |
Summary: | summary |