The following data is part of a premarket notification filed by Shanghai United Imaging Healthcare Co., Ltd. with the FDA for Udr 780i.
Device ID | K173953 |
510k Number | K173953 |
Device Name: | UDR 780i |
Classification | System, X-ray, Stationary |
Applicant | Shanghai United Imaging Healthcare Co., Ltd. No. 2258 Chengbei Rd., Jiading Industrial District Shanghai, CN 201807 |
Contact | Xin Gao |
Correspondent | Xin Gao Shanghai United Imaging Healthcare Co., Ltd. No. 2258 Chengbei Rd., Jiading Industrial District Shanghai, CN 201807 |
Product Code | KPR |
CFR Regulation Number | 892.1680 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2017-12-27 |
Decision Date | 2018-01-26 |
Summary: | summary |
Device Identifier | submissionNumber | Supplement |
---|---|---|
06971576833061 | K173953 | 000 |