510(k) K910274 ยท LGF Component, Cast
ARTIFLEX(TM)
| Applicant | Beiersdorf, Inc., Norwalk CT, US |
| Decision | Substantially Equivalent, Mar 5, 1991 |
| Received | Jan 23, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K910274
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.