510(k) K101824 ยท EZL Catheter, Retention Type, Balloon
AMSURE 3-WAY HYDROPHILIC LATEX FOLEY CATHETER
| Applicant | Amsino International, Inc., Pomona CA, US |
| Decision | Substantially Equivalent, Sep 13, 2010 |
| Received | Jul 1, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K101824
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.