The following data is part of a premarket notification filed by Shanghai Heartcare Medical Technology Co., Ltd. with the FDA for Micro Catheter.
Device ID | K202926 |
510k Number | K202926 |
Device Name: | Micro Catheter |
Classification | Catheter, Percutaneous, Neurovasculature |
Applicant | Shanghai Heartcare Medical Technology Co., Ltd. 590 Ruiqing Rd, Building 4, Suite 201, East Zhangjing High-Tech Park Shanghai, CN 201201 |
Contact | Zongyu Xue |
Correspondent | Diana Hong Mid-Link Consulting Co., Ltd P.O. Box 120-119 Shanghai, CN 200120 |
Product Code | QJP |
CFR Regulation Number | 870.1250 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2020-09-29 |
Decision Date | 2022-02-10 |