The following data is part of a premarket notification filed by Sonoscape Medical Corp. with the FDA for S45 Digital Color Doppler Ultrasound System.
Device ID | K160283 |
510k Number | K160283 |
Device Name: | S45 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 | 2016-02-03 |
Decision Date | 2016-04-04 |
Summary: | summary |
Device Identifier | submissionNumber | Supplement |
---|---|---|
06945868614508 | K160283 | 000 |
06945868601379 | K160283 | 000 |