The following data is part of a premarket notification filed by Neusoft Medical Systems Co., Ltd. with the FDA for Nsm-s15 System.
Device ID | K092237 |
510k Number | K092237 |
Device Name: | NSM-S15 SYSTEM |
Classification | System, Nuclear Magnetic Resonance Imaging |
Applicant | NEUSOFT MEDICAL SYSTEMS CO., LTD. NO.3-11, WENHUA ROAD HEPING DISTRICT Shenyang, Liaoning, CN 110004 |
Contact | Tian Yuehui |
Product Code | LNH |
CFR Regulation Number | 892.1000 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | Yes |
Combination Product | No |
Date Received | 2009-07-23 |
Decision Date | 2009-09-09 |
Summary: | summary |