510(k) K952526 ยท KMF Bandage, Liquid
CUTINOVA CAVITY
| Applicant | Beiersdorf, Inc., Norwalk CT, US |
| Decision | Substantially Equivalent for Some Indications, Aug 14, 1995 |
| Received | Jun 1, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K952526
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.