The following data is part of a premarket notification filed by Sonoscape Company Limited with the FDA for S22 Digital Color Doppler Ultrasound System.
| Device ID | K142815 |
| 510k Number | K142815 |
| Device Name: | S22 Digital Color Doppler Ultrasound System |
| Classification | System, Imaging, Pulsed Doppler, Ultrasonic |
| Applicant | SONOSCAPE COMPANY LIMITED YIZHE BLDG., YUQUAN RD, Nanshan Shenzhen, CN 518051 |
| Contact | Toki Wu |
| Correspondent | Toki Wu SONOSCAPE COMPANY LIMITED YIZHE BLDG., YUQUAN RD, 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 | 2014-09-29 |
| Decision Date | 2015-01-28 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 06945868612214 | K142815 | 000 |
| 06945868612207 | K142815 | 000 |
| 06945868601348 | K142815 | 000 |
| 06945868601287 | K142815 | 000 |
| 06945868601256 | K142815 | 000 |
| 06945868601201 | K142815 | 000 |
| 06945868601195 | K142815 | 000 |
| 06945868601171 | K142815 | 000 |
| 06945868600303 | K142815 | 000 |