The following data is part of a premarket notification filed by Wuxi Hisky Medical Technologies Co., Ltd. with the FDA for Shear Wave Quantificational Ultrasound Diagnostic System.
Device ID | K173595 |
510k Number | K173595 |
Device Name: | Shear Wave Quantificational Ultrasound Diagnostic System |
Classification | System, Imaging, Pulsed Echo, Ultrasonic |
Applicant | Wuxi Hisky Medical Technologies Co., Ltd. Room B401, 530 Plaza, University Science Park, Taihu International Science & Technology Park Wuxi, CN 214135 |
Contact | Jinhua Shao |
Correspondent | Ray Wang Beijing Believe-Med Technology Service Co., Ltd. 5-402, Building #27, No. 56, LiangXiang East Rd., FangShan District Beijing, CN 102401 |
Product Code | IYO |
Subsequent Product Code | ITX |
Subsequent Product Code | IYN |
CFR Regulation Number | 892.1560 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2017-11-21 |
Decision Date | 2018-06-22 |
Summary: | summary |
Device Identifier | submissionNumber | Supplement |
---|---|---|
06971679947023 | K173595 | 000 |
06971679947016 | K173595 | 000 |
06971679945005 | K173595 | 000 |
06971679949072 | K173595 | 000 |
06971679949065 | K173595 | 000 |