510(k) K210509 ยท DWM Apparatus, Suction, Patient Care
Rocket Platinum Cured Cathter
| Applicant | Rocket Medical Plc, Washington, GB |
| Decision | Unknown, Sep 9, 2021 |
| Received | Feb 22, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K210509
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.