The following data is part of a premarket notification filed by Shenzhen Mindray Bio-medical Electronics Co., Ltd. with the FDA for Dc-70/dc-70t /dc-70 Pro/dc-70 Exp/dc-75/dc-78/dc-70s Diagnostic Ultrasound System.
Device ID | K163690 |
510k Number | K163690 |
Device Name: | DC-70/DC-70T /DC-70 Pro/DC-70 Exp/DC-75/DC-78/DC-70S Diagnostic Ultrasound System |
Classification | System, Imaging, Pulsed Doppler, Ultrasonic |
Applicant | Shenzhen Mindray Bio-Medical Electronics Co., Ltd. Keji 12th Road South, Hi-tech Industrial Park Shenzhen, CN 518057 |
Contact | Yang Zhaohui |
Correspondent | Yang Zhaohui Shenzhen Mindray Bio-Medical Electronics Co., Ltd. Keji 12th Road South, Hi-tech Industrial Park Shenzhen, CN 518057 |
Product Code | IYN |
Subsequent Product Code | ITX |
Subsequent Product Code | IYO |
Subsequent Product Code | LLZ |
CFR Regulation Number | 892.1550 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2016-12-28 |
Decision Date | 2017-04-20 |
Summary: | summary |
Device Identifier | submissionNumber | Supplement |
---|---|---|
06944904099590 | K163690 | 000 |
06944904099583 | K163690 | 000 |
06944904099576 | K163690 | 000 |
06944904099569 | K163690 | 000 |
06944904097688 | K163690 | 000 |
06944904088389 | K163690 | 000 |