The following data is part of a premarket notification filed by Neusoft Medical Systems Co., Ltd. with the FDA for Neuviz 16 Multi-slice Ct Scanner System.
Device ID | K092742 |
510k Number | K092742 |
Device Name: | NEUVIZ 16 MULTI-SLICE CT SCANNER SYSTEM |
Classification | System, X-ray, Tomography, Computed |
Applicant | NEUSOFT MEDICAL SYSTEMS CO., LTD. NO.3-11, WENHUA ROAD HEPING DISTRICT Shenyang, Liaoning, CN 110004 |
Contact | Tian Yangfang |
Correspondent | Tamas Borsai TUV RHEINLAND OF NORTH AMERICA, INC. 12 COMMERCE RD. Newton, CT 06470 |
Product Code | JAK |
CFR Regulation Number | 892.1750 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | Yes |
Combination Product | No |
Date Received | 2009-09-08 |
Decision Date | 2009-09-22 |