510(k) K002868 ยท EZL Catheter, Retention Type, Balloon
BARD ALL-SILICONE 3-WAY FOLEY CATHETER; BARD LUBRI-SIL 3-WAY FOLEY CATHETER; BARD LUBRI-SIL I.C. 3-WAY FOLEY CATHETER
| Applicant | C.R. Bard, Inc., Covington GA, US |
| Decision | Substantially Equivalent, Dec 8, 2000 |
| Received | Sep 13, 2000 |
| Type | Abbreviated |
| FDA record | Open on fda.gov |
Recalls that name K002868
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.