510(k) K090262 ยท EZL Catheter, Retention Type, Balloon
PERCUCATH URINARY CATHETER
| Applicant | Percuvision, LLC, Gahanna OH, US |
| Decision | Substantially Equivalent, May 28, 2009 |
| Received | Feb 3, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K090262
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.