510(k) K873295 ยท KOE Dilator, Urethral
PROSTATIC URETHRO. BALLOON DILATATION CATHETER
| Applicant | Medi-Tech, Inc., Watertown MA, US |
| Decision | Substantially Equivalent, Jul 31, 1989 |
| Received | Aug 17, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K873295
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.