The following data is part of a premarket notification filed by Neusoft Medical Systems Co., Ltd. with the FDA for Modification To Superopen 0.35t, Model Nsm-p035.
Device ID | K061132 |
510k Number | K061132 |
Device Name: | MODIFICATION TO SUPEROPEN 0.35T, MODEL NSM-P035 |
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 Yanfang |
Correspondent | Tian Yanfang NEUSOFT MEDICAL SYSTEMS CO., LTD. NO.3-11, WENHUA ROAD HEPING DISTRICT Shenyang, Liaoning, CN 110004 |
Product Code | LNH |
CFR Regulation Number | 892.1000 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2006-04-24 |
Decision Date | 2006-05-24 |
Summary: | summary |