510(k) K183335 ยท GBM Catheter, Urethral
Medline Poly-Cath Red Polymer Urethral Catheter
| Applicant | Medline Industries, Inc., Northfiled IL, US |
| Decision | Substantially Equivalent, Jun 12, 2019 |
| Received | Dec 3, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K183335
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.