510(k) K220920 ยท HAO Instrument, Surgical, Non-Powered
Matreneu Percutaneous Balloon Compression Kit
| Applicant | Shenzhen Shineyard Medical Device Co. , Ltd., Shenzhen, CN |
| Decision | Substantially Equivalent, Sep 7, 2022 |
| Received | Mar 30, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K220920
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.