510(k) K202119 ยท IYO System, Imaging, Pulsed Echo, Ultrasonic
AcuSee AS-P1000 System
| Applicant | Weipeng (Suzhou) Medical Devices Co., Ltd., Suzhou, CN |
| Decision | Substantially Equivalent, Oct 7, 2020 |
| Received | Jul 30, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K202119
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.