510(k) K842890 ยท KOD Catheter, Urological
PERCUFIX CATHETER CUFF
| Applicant | Medi-Tech, Inc., Watertown MA, US |
| Decision | Substantially Equivalent, Sep 4, 1984 |
| Received | Jul 23, 1984 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K842890
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.