510(k) K973572 ยท MDA Elastomer, Silicone, For Scar Management
KELOCOTE SCAR GEL AND KELOCOTE LASER GEL
| Applicant | Hanson Medical, Inc., Kingston WA, US |
| Decision | Substantially Equivalent, Oct 21, 1997 |
| Received | Sep 19, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K973572
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.