The following data is part of a premarket notification filed by Sonoscape Company Limited with the FDA for S12 Digital Color Doppler Ultrasound System.
Device ID | K142474 |
510k Number | K142474 |
Device Name: | S12 Digital Color Doppler Ultrasound System |
Classification | System, Imaging, Pulsed Doppler, Ultrasonic |
Applicant | SONOSCAPE COMPANY LIMITED YIZHE BLDG., YUQUAN RD Shenzhen, CN 518051 |
Contact | Toki Wu |
Correspondent | Toki Wu SONOSCAPE COMPANY LIMITED YIZHE BLDG., YUQUAN RD Shenzhen, CN 518051 |
Product Code | IYN |
Subsequent Product Code | ITX |
Subsequent Product Code | IYO |
CFR Regulation Number | 892.1550 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2014-09-03 |
Decision Date | 2014-12-19 |
Summary: | summary |