510(k) K894883 ยท EZL Catheter, Retention Type, Balloon
PHYCON ALL SILICONE BALLOON CATHETER
| Applicant | Vitaid, Ltd., Ontario, Canada, CA |
| Decision | Substantially Equivalent, Apr 25, 1990 |
| Received | Aug 1, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K894883
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.