The following data is part of a premarket notification filed by Shenzhen Rf Tech Co., Ltd. with the FDA for 8ch Foot Ankle Coil.
Device ID | K160932 |
510k Number | K160932 |
Device Name: | 8ch Foot Ankle Coil |
Classification | Coil, Magnetic Resonance, Specialty |
Applicant | Shenzhen RF Tech Co., Ltd. 2-F, Bld4, Juhui Industrial Park, Tianliao, Guangming Shenzhen, CN 518132 |
Contact | Ke Xi |
Correspondent | Elena Lu Shenzhen Joyantech Consulting Co., Ltd. Room 1122, International Mayors Communication Centre Shenzhen, CN 518000 |
Product Code | MOS |
CFR Regulation Number | 892.1000 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2016-04-04 |
Decision Date | 2016-08-01 |
Summary: | summary |