The following data is part of a premarket notification filed by Sonoscape Medical Corp. with the FDA for P60 Series Digital Color Doppler Ultrasound System.
| Device ID | K171000 |
| 510k Number | K171000 |
| Device Name: | P60 Series Digital Color Doppler Ultrasound System |
| Classification | System, Imaging, Pulsed Doppler, Ultrasonic |
| Applicant | SONOSCAPE MEDICAL CORP. 4/F, 5/F, 8/F, 9/F & 10/F, Yizhe Building, Yuquan Road, Nanshan Shenzhen, CN 518051 |
| Contact | Toki Wu |
| Correspondent | Toki Wu SONOSCAPE MEDICAL CORP. 4/F, 5/F, 8/F, 9/F & 10/F, Yizhe Building, Yuquan Road, Nanshan 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 | 2017-04-03 |
| Decision Date | 2017-07-11 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 06945868616052 | K171000 | 000 |
| 06945868616045 | K171000 | 000 |
| 06945868616038 | K171000 | 000 |
| 06945868616021 | K171000 | 000 |