510(k) K200134 ยท GBM Catheter, Urethral
Jimushi Sterile Urethral Catheter for single use
| Applicant | Hangzhou Jimushi Meditech Co., Ltd., Hangzhou, CN |
| Decision | Substantially Equivalent, Jun 1, 2020 |
| Received | Jan 21, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K200134
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.