510(k) K183461 ยท GBM Catheter, Urethral
Rusch Flocath Hydrophilic Intermittent Catheter, Rusch MMG Hydrophilic Intermittent Catheter
| Applicant | Teleflexmedical, Inc., Morrisville NC, US |
| Decision | Unknown, May 8, 2019 |
| Received | Dec 14, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K183461
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.