510(k) K915253 ยท IWA Source, Wire, Iridium, Radioactive
IR-192 IMPLANT, MODIFICATION
| Applicant | Omnitron Intl., Inc., Lajke Charles LA, US |
| Decision | Substantially Equivalent, Feb 27, 1992 |
| Received | Nov 18, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K915253
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.