The following data is part of a premarket notification filed by Sonoscape Company Limited with the FDA for S8 Exp Portable Digital Color Doppler Ultrasound System.
| Device ID | K132768 |
| 510k Number | K132768 |
| Device Name: | S8 EXP PORTABLE DIGITAL COLOR DOPPLER ULTRASOUND SYSTEM |
| Classification | System, Imaging, Pulsed Doppler, Ultrasonic |
| Applicant | SONOSCAPE COMPANY LIMITED YIZHE BLDG, YUQUAN ROAD Shenzhen, Guangdong, CN 518051 P.r |
| Contact | Toki Wu |
| Correspondent | Toki Wu SONOSCAPE COMPANY LIMITED YIZHE BLDG, YUQUAN ROAD Shenzhen, Guangdong, CN 518051 P.r |
| Product Code | IYN |
| Subsequent Product Code | ITX |
| Subsequent Product Code | IYO |
| CFR Regulation Number | 892.1550 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2013-09-04 |
| Decision Date | 2013-10-04 |
| Summary: | summary |