510(k) K201720 ยท DQX Wire, Guide, Catheter
LiPPS Analyzer, LiPPS Wire Pressure Guide Wire
| Applicant | Beijing Bywave Sensing Medical Technology Co., Ltd., Beijing, CN |
| Decision | Substantially Equivalent, Feb 18, 2021 |
| Received | Jun 23, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K201720
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.