510(k) K973730 ยท MIB Elastomer, Silicone Block
DURASIL I AND DURASIL II
| Applicant | Hanson Medical, Inc., Seattle WA, US |
| Decision | Substantially Equivalent, Dec 24, 1997 |
| Received | Sep 30, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K973730
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.