510(k) K962611 ยท KOE Dilator, Urethral
BARD EAGLE INFLATION DEVICE
| Applicant | Ryder Intl. Corp., Arab AL, US |
| Decision | Substantially Equivalent, Oct 21, 1996 |
| Received | Jul 3, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K962611
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.