The following data is part of a premarket notification filed by Neusoft Digital Medical Systems Co., Ltd. with the FDA for Superopen 0.23t, Model Nam-p023a.
Device ID | K033315 |
510k Number | K033315 |
Device Name: | SUPEROPEN 0.23T, MODEL NAM-P023A |
Classification | System, Nuclear Magnetic Resonance Imaging |
Applicant | NEUSOFT DIGITAL MEDICAL SYSTEMS CO., LTD. NO.3-11, WENHUA ROAD HEPING DISTRICT Shenyang, Liaoning, CN 110004 |
Contact | Wang Zhiqiang |
Correspondent | Heinz-joerg Steneberg TUV RHEINLAND OF NORTH AMERICA, INC. 12 COMMERCE RD. Newton, CT 06470 |
Product Code | LNH |
CFR Regulation Number | 892.1000 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | Yes |
Combination Product | No |
Date Received | 2003-10-15 |
Decision Date | 2003-10-29 |
Summary: | summary |