The following data is part of a premarket notification filed by Sonoscape Company Limited with the FDA for Digital Color Doppler Ultrasound System.
| Device ID | K130801 |
| 510k Number | K130801 |
| Device Name: | DIGITAL COLOR DOPPLER ULTRASOUND SYSTEM |
| Classification | System, Imaging, Pulsed Doppler, Ultrasonic |
| Applicant | SONOSCAPE COMPANY LIMITED 4/F YIZHE BLDG, YUQUAN ROAD Shenzhen, Guangdong, CN 518051 |
| Contact | Toki Wu |
| Correspondent | Toki Wu SONOSCAPE COMPANY LIMITED 4/F YIZHE BLDG, YUQUAN ROAD Shenzhen, Guangdong, 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 | 2013-03-22 |
| Decision Date | 2013-06-14 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 06945868613013 | K130801 | 000 |
| 06945868613006 | K130801 | 000 |